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Damodharan, N.
- Isolation and Screening the Pharmacological Activities of Vegetative and Spore-Crystal Proteins from Bacillus thuringiensis
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1 Department of Pharmaceutics, SRM College of Pharmacy, SRM University, Kattankulathur, Tamil Nadu, IN
1 Department of Pharmaceutics, SRM College of Pharmacy, SRM University, Kattankulathur, Tamil Nadu, IN
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Research Journal of Pharmacy and Technology, Vol 11, No 1 (2018), Pagination: 38-40Abstract
Bacillus thuringiensis, the most successful and most widely used microbial insecticide, produces crystal proteins. The physiological significance of the crystal proteins poorly understood except for the potent insecticidal activity. In the current study, an attempt made to isolate vegetative and spore-crystal proteins from Bacillus thuringiensis NCIM2514 and to perform their hemolytic and antioxidant activities. The proteins were separated by salting out methods then by using SDS-PAGE. The molecular protein weight of the vegetative and spore-crystal protein identified as the presence of low molecular weight protein. Pharmacological activities as antioxidant and hemolytic studies were performed for the crude proteins and found as Spore-crystal proteins contain more anti-oxidant when compared to vegetative proteins.Keywords
Bacillus thuringiensis (Bt), Spore-Crystal Proteins, Vegetative Proteins. SDS-PAGE, Antioxidant.References
- Akiba T, Abe Y, Ktada S, Kusaka Y, Ito A, Ichimatsu T, Katayaman H, Akao T, Higuchi K, Mizuki E, Ohba M, Kanai R and Harata K. Crystal structure of the parasporin-2 Bacillus thuringiensis toxin that recognizes cancer cells. Journal of Molecular Biology. 2009; 386 (1): 121-33.
- Aronson AI and Shai Y. Why Bacillus thuringiensis insecticidal toxins are so effective: unique features of their mode of action. FEMS Microbiology Letters. 2001; 195: 1-8.
- Baum JA, Johnson TB and Carlton BC. Bacillus thuringiensis: Natural and recombinant bioinsecticide products. In: Biopesticides: Use and Delivery, Hall FR and Menn JJ, Eds, Humana Press 1999, Totowa, NJ, 189-210.
- Becker N. Bacterial control of vector mosquitoes and black flies In: Entomopathogenic Bacteria: From Laboratory to Field Application. Charles JF, Delecluse A, Neilson-LeRoux (Eds). Dordrecht, Kluwer Academic Publishers 2000; 383-98.
- Capello M, Bungiro RD, Harrison LM, Bischof LT, Griffitts JS, Barrows BD and Aroian RV. A purified Bacillus thuringiensis crystal protein with therapeutic activity against the hookworm parasite Ancylostomaceylanicus. Proc Natl AcadSci USA 2006; 103: 15154-9.
- Crickmore N, Zeigler DR, Feitelson J, Schnepf E, Van Rie J, Lereclus D, Baum J and Dean DH. Revision of the literature for the Bacillus thuringiensis pesticidal crystal proteins. Microbiology Molecular Biology Review 1998; 62: 807-13.
- Jung YC, Mizuki E, Akao T and Cote JC. Isolation and characterization of a novel Bacillus thuringiensis strain expressing a novel crystal protein with cytocidal activity against human cancer cells. Journal of Applied Microbiology. 2007; 103: 65-79.
- Katayama H, Kusaka Y, Yokota H, Akao T, Kojima M, Nakamura O, Mekada E and Mizuki E. Parasporin-1, a novel cytotoxic protein from Bacillus thuringiensis, induces Ca2+ influx and a sustained elevation of the cytoplasmic Ca2+ concentration in toxin-sensitive cells. Journal of Biological Chemistry. 2007; 282: 7742-52.
- Kitada S, Abe Y, Shimada H, Kusaka Y, Matsuo Y, Katayama H, Okumura S, Akao T, Mizuki E, Kuge O, Sasaguri Y, Ohba M and Ito A. Cytocidal actions of parasporin2, an anti-tumour crystal toxin from Bacillus thuringiensis. Journal of Biological Chemistry 2006; 281(36): 26350-60.
- Mizuki E, Ohba M, Akao T, Yamashita S, Saitoh H and Park YS. Unique activity associated with non-insecticidal Bacillus thuringiensis parasporal inclusions: in vitro cell-killing action on human cancer cells. Journal of Applied Microbiology. 1999; 86: 477-86.
- Mizuki E, Park YS, Saitoh H, Yamashita S, Akao T, Higuchi K and Ohba M. Parasporin, a human leukaemic cell-recognizing parasporal protein of Bacillus thuringiensis. Clinical and Diagnostic Laboratory Immunology. 2000; 7: 625-34.
- pH-Responsive Polymers and its Application in Drug Delivery System and Pharmaceutical Field
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Authors
Affiliations
1 Department of Pharmaceutics, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai –603202, IN
2 Department of Pharmaceutics, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai – 603202, IN
1 Department of Pharmaceutics, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai –603202, IN
2 Department of Pharmaceutics, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai – 603202, IN
Source
Research Journal of Pharmacy and Technology, Vol 12, No 2 (2019), Pagination: 944-958Abstract
Stimuli-sensitive polymers which are also called as ‘smart polymers' are rapidly acquiring popularity in the field of self-regulated and control release drug delivery system. Control drug delivery system is used which enable to obtain better drug product with greater safety, efficacy, and reliability. Stimuli-responsive polymers (smart polymers) are the large molecules which in response to environmental factor like, light, heat, ionic and magnetic field reveals peculiar physiochemical changes. The review summarizes the recent development explaining different types of synthesis, its characteristics, the principle of working, and its application in various fields. Several polymers with its potential uses in control drug delivery, personal, human care, biological and membrane science as well as its application in the pharmaceutical field are explained below. They have been playing a vital role in various fields since last three decades. In the field of chemistry and biology, pH-sensitive materials having multi-characteristics nature makes a promising role. It also describes about an important use of pH-sensitive polymer in different therapy like gene therapy and the applicability of system as insulin delivery in consideration of physiochemical properties of these smart polymers. Apart of drug delivery, It has also an important application in purification and separation of molecules like enzyme, protein, peptides (Chromatographic studies).Keywords
pH-Sensitive Polymer, Liposomes, Drug Delivery, Polymethacrylic Acid, Poly (Acrylic Acid).References
- Balamuralidhara V et al., pH-sensitive sensitive drug delivery system. American Journal of Drug Discovery and Development.2011; 1(1):24-48.
- Ying-Jie Zhu and Feng Chen. pH - Responsive Drug-Delivery Systems. Chemistry An Asian Journal.2014;10:1-23.
- Panja N, Chattopadhyam A.K., New oil modified acrylic polymer for pH sensitive drug release: Experimental results and statistical analysis. Journal of advance in natural science, 2014;3.
- Shaik MR, Korsapati M, Panati D. Polymers in Controlled Drug Delivery systems International journal of pharma science.2012; vol.2 :112-116.
- Vilar G, Tulla-puche j and Alberico Fernando. Polymer and Drug Delivery System. Current Drug Delivery. 2012; 9:000-000.
- Nakamura et al., Uptake and Release of Budesonide from Mucoadhesive. pH sensitive Copolymers and their Application to Nasal delivery. Control Release Journal.1999; 61:329-335.
- Iwata, McGinity M and J.W. Dissolution, Stability, and Morphological Properties of Conventional and Multiphase poly (DL-lactic-co-glycolic acid) Microspheres containing water-soluble Compounds. Pharmaceutical Research journal.1993; 10:1219-1227.
- Vaida C et al., Microparticles for Drug Delivery based on Functional Polycaprolactones with Enhanced Degradability Loading of Hydrophilic and Hydrophobic Active compounds. Macromolecular Bioscience. 2010; 10: 925-933.
- Yoshida Takayuki (PhD), Lai Tsz chung , Skwon Glen, and Kazuhiro. pH- and Ion-Sensitive Polymers for Drug Delivery. Expert Opinion of Drug Delivery. 2013 November; 10(11): 1497–1513.
- Kocak, G, Tuncer, C, Butun V. pH responsive polymer. Polymer Chemistry. 2016; 8: 144-176.
- Reyes-ortega F. Institute of Polymer Science and Technology (ICTP-CSIC), Spain and Networking Biomedical Research Center in Bioengineering, Biomaterials and Nano-medicine (CIBER-BBN), Spain. Woodhead Publishing. 2014; 1:47- 55.
- Melendez - ortiz, Ivan H, Varca HC. State of Smart Polymers: from Fundamentals to final Application. Polymer Science: Research Advances, Practical Application and Educational Aspects. Formatex research Center . 2016; 1:476-487.
- Kang SI. and Bae YH. pH - Induced Solubility Transition of Sulfonamide Based Polymers. Journal of Controlled Release. 2002; 80:145–155.
- Zhao Y et al., Self-assembled pH Responsive Hydrogels Composed of the RATEA16 peptide. Biomacromolecules. 2008; 9:1511–1518.
- Vyas SP, k.khar Roop. Controlled drug delivery concept and advances. Edition 2002. Vallabh prakashan, 21. November 2001;105.
- Sonia T A. and Sharma CP. An overview of Natural Polymers for Oral Insulin delivery. Drug Discovery Today. 2012; 17: 784–792.
- Hoffman AS, Synthetic Hydrogels for Biomedical Applications. Advance Drug Delivery Reviews. 2012; 64: 18–23.
- Alvarez-Lorenzo et al., Multi-Response Optimization in the Formulation of a Topical Cream from Natural Ingredients. Advance Drug Delivery Reviews.2013; 65: 1148–1171.
- Samal SK et al., Cationic Polymers and their Therapeutic Potential. American Chemical Society Review. 2012; 41:7147–7194.
- Santos J.R, Alves N.M and Mano J.F, Properties and in vitro drug release of pH- and temperature-sensitive double cross-linked interpenetrating polymer network hydrogels based on hyaluronic acid/poly (N-isopropylacrylamide) for transdermal delivery of luteolin. Bioactive Journal of Compatible Polymer. 2010; 25: 169–184.
- Cao N et al., Dendritic porous SNO2/ SiO2 @polymer nanospheres/pH controlled styptic drug releaseJournal of Industrial Engineering Chemistry., 2016; 34: 9–13.
- Mansour Heidi M et al.,. Materials for Pharmaceutical Dosage Forms. International Journal of Molecular Sciences. 15 September 2010; 11:3302.
- Wei L et al., Dual-drug delivery system based on hydrogel/ micelle composites. Biomaterials. 2009; 30: 2606–2613.
- Sawayanagi,Y., Nambu N and Nagai T. Direct compressed tablets containing chitin Chemistry of Pharmaceutical Bulletin. 1982; 30(11): 4216.
- Upadrashta S.M., Katikaneni P. R. and Nuessle N.O. Chitin and Chitosan as Disintegrants in Paracetamol Tablets. Drug Development and Industrial Pharmacy. 1992 ; 18:1701.
- Ozbas-Turan, Akbuga S, Aral JC. Controlled Release of Interleukin-2 from Chitosan microspheres. Journal of Pharmaceutical Science. 2002; 91:1245–1251.
- Chena Sung-Ching et al., A novel pH-sensitive hydrogel composed of N,O-carboxymethyl chitosan and alginate cross-linked by genipin for protein drug delivery. Journal of Controlled Release. 2004;2: 286.
- Hu S. G. Jou C. H. and Yang M. C. Protein adsorption, fibroblast activity and antibacterial properties of poly (3-hydroxybutyric acid-co-3-hydroxyvaleric acid) grafted with chitosan and chitooligosaccharide after immobilized with hyaluronic acid. Biomaterials. 2003 ;24: 2685–2693.
- Hillyard I W. Doczi J. and Kierman P. B. Carbohydrate Polymers. Proceedings of the Society for experimental Experimental biology and medicine. 1964; 115:1108.
- Acikgoz M et al., Chitosan microspheres of diclofenac sodium. Pharmazie. 1995; 50:273.
- DAyala, G.G; Malinconico M, Laurienzo P. Marine derived polysaccharides for biomedical applications: chemical modification approaches. Molecules .2008; 13(9): 2069–2106.
- Pajic-Lijakovic I et al., Investigation of Ca-alginate hydrogel rheological behaviour in conjunction with immobilized yeast cell growth dynamics. Journal of Microencapsulation. 2007; 24:420–429.
- Yang L. and Liu H. Stimuli-responsive magnetic particles and their applications in biomedical field. Powder Technology. 2013; 240: 54–65.
- El-Sherbiny IM. Enhanced pH-responsive carrier system based on alginate and chemically modified carboxymethyl chitosan for oral delivery of protein drugs: Preparation and in-vitro assessment. Carbohydrate Polymers. 2010; 80: 1125–1136.
- Silva C M et al., Alginate microspheres prepared by internal gelation: development and effect on insulin stability. International Journal of Pharmaceutics. 2006; 311: 1–10.
- Liao YH et al., Hyaluronan: pharmaceutical Characterization and drug delivery. Drug Delivery. 2005; 12: 327–342.
- Kang JY et al., Novel porous matrix of hyaluronic acid for the three-dimensional culture of chondrocytes. International Journal of Pharmaceutics. 2009; 369: 114–120.
- Malafaya PB, Silva GA, Reis RL. Natural-origin polymers as carriers and scaffolds for biomolecules and cell delivery in tissue engineering applications. Advance Drug Delivery Review. 2007; 59: 207–233.
- Collins MN and Birkinshaw C. Hyaluronic acid based scaffolds for tissue Engineering – a review. Carbohydrate Polymers. 2013; 92: 1262–1279.
- Khademhosseini A Ji C and Dehghani F. Enhancing cell penetration and proliferation in chitosan hydrogels for tissue engineering applications. Biomaterials. 2011; 32: 9719–9729.
- Guragain S et al., Multi-Stimuli-Responsive Polymeric Materials. Chemistry European Journal. 2015; 21:13164–13174.
- Wang L et al ., Triple-responsive hydrogels: Synthesis and controlled drug delivery. Reactive and Functional Polymer. 2010; 70: 159–167.
- Jiang FJ et al., Polymer. Frontiers of Physics. 2016; 83: 85–91.
- Achilleos DS. and Vamvakaki M.. Multiresponsive Spiropyran-Based Copolymers Synthesized by Atom Transfer Radical Polymerization. Macromolecules. 2010; 43(17):7073–7081.
- Wu W et al., Multifunctional Hybrid Nanogel forIntegration of Optical Glucose Sensing and Self-Regulated Insulin Release at Physiological pH . American Chemical Society Nano. 2010; 4:4831–4839.
- Jiang G et al., Preparation of multi-responsive micelles for controlled release of insulin. Colloid Polymer Science. 2015; 293: 209–215.
- Ma et al., Construction of N-halamine labeled silica/zinc oxide hybrid nanoparticles for enhancing antibacterial ability of Ti implants Polymer. Journal of Polymer Science Part A: Polymer Chemistry. 2011; 49: 2725–2733.
- Kim SJ et al., Electrical response characterization of interpenetrating polymer network hydrogels as an actuator Sensitive Actuators, American Chemical Society Journal 2004; 115:146–150.
- Wei CA, Guo J. and Wang CC. Preparation and Characterization of Polyfluorene-Based Supramolecular π-Conjugated Polymer Gels.Macromolecular chemistry and physics. Rapid Communication. 2011; 32: 451–455.
- Li DW, Bu YZ, Zhang LN, Wang X, Yang YY, Zhuang YP, Yang F, Shen H. and Wu DC. Facile Construction of pH- and Redox- Responsive Micelles from a Biodegradable Poly(β-hydroxyl amine) for Drug Delivery. Biomacromolecules. 2016; 17: 291–300.
- Kashyap S et al., Enzyme and Thermal Dual Responsive Amphiphilic Polymer Core-Shell Nanoparticle for Doxorubicin Delivery to Cancer Cells. Biomacromolecules. 2016; 17: 384–398.
- Wang B, Liu HJ, Jiang TT, Li QH. and Chen Y. Thermo-, and pH dual-responsive poly(N-vinylimidazole): Preparation, characterization and its switchable catalytic activity. Polymer. 2014; 55: 6036–6043.
- Liu Y et al., Self-assembled micellar nanoparticles of a novel star copolymer for thermo and pH dual-responsive drug release. Journal of Colloid Interface Science. 2009; 329: 244–252.
- González N, Elvira C. and Román JS. Novel Dual-Stimuli-Responsive Polymers Derived from Ethylpyrrolidine. Macromolecules. 2005; 38: 9298–9303.
- Schilli CM et al., A New Double-Responsive Block Copolymer Synthesized via RAFT Polymerization: Poly(N-isopropylacrylamide)-block-poly(acrylic acid). Macromolecules. 2004; 37, 7861–7866.
- Zhang W et al., Micellization of Thermo- and pH-Responsive Triblock Copolymer of Poly(ethylene glycol)-b-poly(4-vinylpyridine)-b-poly(N-isopropylacrylamide). Macromolecules, 2005; 38:8850–8852.
- Zhang Y, Wu T. and Liu S. Micellization Kinetics of a Novel Multi – Responsive Double Hydrophillic Diblock Copolymer Studied by Stopped Flow. Macromolecular Chemistry and Physics. 2007; 208:2492–2501.
- Taktak FF. and Butun V. Synthesis and physical gels of pH-and thermo-responsive tertiary amine methacrylate based ABA triblock copolymers and drug release studies Polymer, 2010; 51(16):3618– 3626.
- Han X et al., Effect of Composition of PDMAEMA-b-PAA Block Copolymers on Their pH- and Temperature-Responsive Behaviors. Langmuir .2013; 29:1024–1034.
- Butun V, Billingham NC and Armes SP., Synthesis and aqueous solution properties of novel hydrophilic–hydrophilic block copolymers based on tertiary aminemethacrylates. Chemical Communication.1997; 671–672.
- Butun V, Armes SP and Billingham NC. Polymer, Synthesis and aqueous solution properties of near-monodisperse tertiary amine methacrylate homopolymers and diblock copolymers. Polymer, 2001; 42(14): 5993–6008
- Ge ZS and Liu SY. Facile Fabrication of Multistimuli‐Responsive Metallo Supramolecular Core Cross‐Linked Block Copolymer Micelles Macromolecular Rapid Communication. 2013; 34: 922–930.
- Li CH et al., Synthesis and Self-Assembly of Coil−Rod Double Hydrophilic Diblock Copolymer with Dually Responsive Asymmetric Centipede-Shaped Polymer Brush as the Rod Segment. Macromolecules, 2009; 42: 2916–2924.
- Liu L et al., Independent temperature and pH dual-stimuli responsive yolk/shell polymer microspheres for controlled release: Structural effect. European Polymer Journal. 2015; 69: 540–551.
- Zhang YF et al., Cationic methacrylate copolymers containing primary and tertiary amino side groups: Controlled synthesis via RAFT polymerization, DNA condensation, and in vitro gene transfection Journal of Polymer Science Part A: Polymer Chemistry. 2008; 46: 2379–2389.
- Deng L et al., Synthesis of well-defined poly(N-isopropylacrylamide)-b-poly(L-glutamic acid) by a versatile approach and micellization Journal of Colloid Interface Science. 2008; 323:169–175.
- Tuncer C et al., Multi-responsive microgel of a water-soluble monomer via emulsion polymerization. Journal of Applied Polymer Science. 2015; 132: 42072.
- Butun V et al., Abstract Paper. American Chemical Society. 1999; 218, U443–U443.
- Butun V, Armes SP and Billingham NC. Selective quaternization of 2-(dimethylamino) ethyl methacrylate residues in tertiary amine methacrylate diblock copolymers. Macromolecules.2001; 34:1148–1159.
- Butun V. Selective betainization of 2-(dimethylamino) ethyl methacrylate residues in tertiary amine methacrylate diblock copolymers and their aqueous solution properties . Polymer, 2003; 44: 7321–7334.
- Webster OW et al., Group-transfer polymerization. 1. A new concept for addition polymerization with organosilicon initiators. Journal of American Chemical Society. 1983; 105: 5706–5708.
- Sheng Dai, a Palaniswamy Ravib and Kam Chiu Tam. pH-Responsive polymers: synthesis, properties and applications. The royal society of chemistry. 2007; 4: 435-436.
- Odian G, Principles of Polymerization, John Wiley and Sons, Inc.,Hoboken. New York. 4th edn. Volume 1 2004.
- Matyjaszewski K and Davis T.P., Handbook of Radical Polymerization, John Wiley and Sons, Inc. Hoboken. South wales. 2002.
- Tan BH et al., Microstructure and rheological properties of pH-responsive core–shell particles. Polymer. 2005; 46: 10066–10076.
- Tirtaatmadja V, Tam KC and R. D. Jenkins RD. Rheological Properties of Model Alkali-Soluble Associative (HASE) Polymers: Effect of Varying Hydrophobe Chain Length Macromolecules. 1997; 30: 3271–3282.
- Dai S et al., Light Scattering of Dilute Hydrophobically Modified Alkali-Soluble Emulsion Solutions: Effects of Hydrophobicity and Spacer Length of Macromonomer. Macromolecules, 2000; 33: 7021–7028.
- Tan BH et al., Microstructure of Dilute Hydrophobically Modified Alkali Soluble Emulsion in Aqueous Salt Solution. Advance Colloid Interface Science. 2005; 113: 111–120.
- T. Fonseca et al., Preparation and Surface Characterization of Polymer Nanoparticles Designed for Incorporation into Hybrid Materials. Langmuir. 2007; 23:5727–5734.
- Patrickios CS et al., ABC triblock polymethacrylates: Group transfer polymerization synthesis of the ABC, ACB, and BAC topological isomers and solution characterization. Journal of Polymeric Science Part A: Polymeric Chemistry. 1998; 36, 617–631.
- Butun V et al., Synthesis and characterization of branched water-soluble homopolymers and diblock copolymers using group transfer polymerization. Macromolecules, 2005; 38(12):4977–4982.
- Amalvy JI et al., Synthesis of sterically stabilized polystyrene latex particles using cationic block copolymers and macromonomers and their application as stimulus-responsive particulate emulsifiers for oil-in-water emulsions. Langmuir. 2004; 20: 4345–4354.
- Butun V, Top RB and Ufuklar S. Synthesis and characterization of novel “schizophrenic” water-soluble triblock copolymers and shell cross-linked micelles. Macromolecules. 2006; 39(3), 1216–1225.
- Butun V, Taktak FF and Tuncer C. Tertiary Amine Methacrylate-Based ABC Triblock Copolymers: Synthesis, Characterization, and Self-Assembly in both Aqueous and Nonaqueous Media Macromolecular Chemistry and Physics. 2011; 212(11):1115–1128.
- Tuncer C and Butun V. Highly cross-linked soluble star copolymers with well controlled molecular weights. European Polymer journal.2015; 67: 292–303.
- Stavrouli N et al., Controlled and Living Polymerization. Macromolecular Rapid Communication. 2007; 28: 560–566.
- Patrickios CS et al., Diblock, ABC triblock, and random methacrylic polyampholytes: synthesis by group transfer polymerization and solution behaviour. Macromolecules. 1994; 27: 930–937.
- Matyjaszewski K. Controlled radical polymerization: state of the art in 2008.In: Controlled/Living Radical Polymerization: Progress in ATRP. American Chemical Society. 2009; 1023: 3–13.
- Lee SB, Russell AJ and Matyjaszewski K. ATRP Synthesis of Amphiphilic Random, Gradient, and Block Copolymers of 2-(Dimethylamino)ethyl Methacrylate and n-Butyl Methacrylate in Aqueous Media. Biomacromolecules. 2003; 4: 1386–1393.
- P. Zhou P et al., Self-assemblies of the six-armed star triblock ABC copolymer: pH- tunable morphologies and drug release. Polymer Chemistry. 2015; 6: 2934–2944.
- Zhang WD et al. Miktoarm star copolymers via combination of RAFT arm‐first technique and aldehyde–aminooxy click reaction. Journal of Polymeric. Science. Part A: Polymeric Chemistry. 2009; 47: 6304–6315.
- Yang YQ et al., pH-sensitive micelles self-assembled from multi-arm star triblock co-polymers poly(ε-caprolactone)-b-poly(2-(diethylamino)ethyl methacrylate)-b-poly(poly(ethylene glycol) methyl ether methacrylate) for controlled anticancer drug delivery. Acta Biomaterialia. 2013; 9: 7679–7690.
- Medel S et al., Thermo- and pH responsive gradient and block copolymers based on 2-(2-methoxyethoxy)ethyl methacrylate synthesized via atom transfer radical polymerization and the formation of thermoresponsive surfaces. Journal of Polymer Science, Part A: Polymer Chemistry 2011; 49 (3): 690-700.
- Gao T et al., Grafting polymer brushes on graphene oxide for controlling surface charge states and templated synthesis of metal nanoparticles. Journal of Applied Polymer Science. 2013; 127(4):3074–3083.
- Abu-Lail NI et al., Micro-cantilevers with end-grafted stimulus-responsive polymer brushes for actuation and sensing.Sensors and Actuators B. 2006; 114(1): 371–378.
- Hu H et al., Synthesis and characterization of the environmental‐sensitive hyperbranched polymers as novel carriers for controlled drug release. Journal of Applied Polymer Science. 2006; 101(1): 311–316.
- Meijs GF, E. Rizzardo E and Thang SH. Radical addition-fragmentation chemistry in polymer synthesis. Polymer Bulletin journal. 1990; 24:501–505.
- Meijs GF, Rizzardo E and Thang SH. Preparation of controlled-molecular-weight, olefin-terminated polymers by free radical methods. Chain transfer using allylic sulfides Macromolecules. 1988; 21:3122–3124.
- Cacioli P et al., Copolymerization of ω-Unsaturated Oligo(Methyl Methacrylate): New Macromonomers. Journal of Macromolecular Science Part A. 1986; 23: 839–852.
- Gregory A. and Stenzel M H. Complex polymer architectures via RAFT polymerization: From fundamental process to extending the scope using click chemistry and nature’s building blocks. Progress in Polymer Science (Oxford). 2012; 37:38–105.
- Smith A E. Xu X. and Mccormick C L. Stimuli-responsive amphiphilic (co)polymers via RAFT polymerization. Progress in Polymer Science. 2010; 35: 45–93.
- Lowe A B. and Mccormick C L. Reversible addition-fragmentation chain transfer (RAFT) radical polymerization and the synthesis of water- soluble(co)polymers under homogeneous conditions in organic and aqueous media. Progress in Polymer Science. 2007; 32: 283–351.
- Lovett JR et al., pH-Responsive Non-Ionic Diblock Copolymers: Ionization of Carboxylic Acid End-Groups Induces an Order–Order Morphological Transition. Angewandte Chemie (International Ed. in English) .2015; 54:1279–1283.
- Dupin D et al., Efficient synthesis of sterically stabilized pH-responsive microgels of controllable particle diameter by emulsion polymerization. Langmuir . 2006; 22(7): 3381–3387.
- Saunders BR, Crowther HM and B. Vincent B. Poly[(methyl methacrylate)-co-(methacrylic acid)] Microgel Particles: Swelling Control Using pH, Cononsolvency, and Osmotic Deswelling. Macromolecules. 1997; 30: 482–487.
- Deka SR et al., Acidic pH-responsive nanogels as smart cargo systems for the simultaneous loading and release of short oligonucleotides and magnetic nanoparticles. Langmuir, 2010; 26:10315– 10324.
- Liechty WB, Scheuerle RL and Peppas NA. Tunable responsive nanogels containing t-butyl methacrylate and 2-(tbutylamino)ethyl methacrylate. Polymer. 2013; 54: 3784–3795.
- Almeida Hugo, Helena Amaral Maria and Lobão Paulo. Temperature and pH stimuli-responsive polymers and their applications in controlled and selfregulated drug delivery. Journal of pharmaceutical science. 2012; 2(6): 01-10.
- Aguilar MR et al., Aguilar t al. Smart Polymers and Their Applications as Biomaterials. Topics in Tissue Engineering. Eds. N Ashammakhi, R Reis and E Chiellini. Woodhead Publishing. 2007; 3.
- Chourasia MK, Jain SK. Pharmaceutical approaches to colon targeted drug delivery systems. Journal of Pharmaceutical Science. 2003; 6: 33-66.
- Chourasia MK, Jain SK. Polysaccharides for colon targeted drug delivery. Drug Delivery 2004; 11(12):9-148.
- Ashish J. Colon Targeting Using pH Sensitive Materials. Advance Research of Gastroenterology and Hepatology. 2018; 8(5): 555748.
- Mishra S. Formulation and evaluation of pH sensitive nanoparticles for colon targeted drug delivery system, 3rd International Conference and Exhibition on Pharmaceutics and Novel Drug Delivery Systems Hilton Chicago/Northbrook, USA. 2013; 2(2):169.
- Jain A. Quasi emulsion spherical crystallization technique based environmentally responsive Tulsion® (pH dependent) microspheres for colon specific delivery. Journal of applied biomedicine. 2016; 14(2):147-155.
- Shi X et al. In vitro and in vivo study of pH-sensitive and colon-targeting P(LE-IA- MEG) hydrogel microspheres used for ulcerative colitis therapy. European Journal of Pharmacy and Biopharmaceutics. 2017; 122: 70-77.
- Agrawal D et al., Formulation and charecterisation of colon targeted pH dependent microspheres of capecitabine for colorectal cancer. Journal of drug delivery and Therapeutics. 2013; 3(6): 215-222.
- Gil ES, Hudson SM. Stimuli-responsive polymers and their bioconjugates. Progression Polymer Science. 2004; 29(12):1173-1222.
- Ruel-Gariépy E, Leroux J. In situ-forming hydrogels-review of temperature-sensitive systems. European Journal of Pharmacy and Biopharmaceutics. 2004; 58(2):409-426.
- Godbey WT, Mikos AG. Recent progress in gene delivery using non-viral transfer complexes. Journal of Control Release. 2001; 72:115-125.
- Borchard G. Chitosans for gene delivery. Advance Drug Delivery Review 2001; 52: 145-150.
- Leong KW et al., DNA-polycation nanospheres as non-viral gene delivery vehicles. Journal of Control Release. 1998; 53: 183-193.
- Henry SM et al., pH-responsive poly (styrene-alt-maleic anhydride) alkylamide copolymers for intracellular drug delivery. Biomacromolecules. 2006; 7: 2407–2414.
- Pack DW et al., Design and development of polymers for gene delivery. Nature Reviews Drug Discovery. 2005; 4: 581–593.
- Grainger ST and El-Sayed MEH. Stimuli-sensitive particles for drug delivery. Biologically-responsive hybrid biomaterials: a reference for material scientists and bioengineers. World Scientific Publishing Co. Pte. Ltd, Danvers. 2010; 171-189.
- Jeong B, Gutowska A. Lessons from Nature: stimuli-responsivepolymers and their biomedical applications. Trends Biotechnology. 2002; 20 (7):305-310.
- Hu J and Liu S. Responsive Polymers for Detection and Sensing Applications: Current Status and Future Developments. Macromolecules, 2010; 43: 8315–8330.
- Kulkarni SS., Aloorkar NH. Smart polymers in drug delivery: an overview. Journal of pharmaceutical Research. 2010; 3(1):100-108.
- Fogueri LR, Singh S. Smart polymers for controlled delivery of proteins and peptides: A review of patents. Recent Patent Drug Delivery Formulation. 2009; 3(1):40-48.
- Torres-Lugo M. and Peppas NA. Transmucosal delivery systems for calcitonin:A review. Biomaterials. 2000; 21: 1191–1196.
- Herber S et al., Miniaturizedcarbon dioxide gas sensor based on sensing of pH-sensitive hydrogel swelling with a pressure sensor. Biomedical Microdevices. 2005; 7:197–204.
- Morishita M et al., Elucidation of the mechanism of incorporation of insulin in controlled release systems based on complexation polymers. Journal of Control Release. 2002; 81(1-2):25-32.
- Foss AC et al., Development of acrylic-based copolymers for oral insulin delivery. European Journal of Pharmacy and Biopharmaceuticals. 2004; 57(2):163-169.
- Terefe NS et al., Application of stimuli-Responsive Polymers for Sustainable Ion Exchange Chromatography. Food and Bioproducts Processing. 2014; 92: 208–225.
- Floating Osmotic Drug Delivery System:A Review
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1 SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai, IN
2 Department of Pharmaceutics, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai, IN
1 SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai, IN
2 Department of Pharmaceutics, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai, IN
Source
Research Journal of Pharmacy and Technology, Vol 12, No 2 (2019), Pagination: 959-971Abstract
Floating Osmotic Drug Delivery System (FODDS) is a controlled oral drug delivery system which comes under the category of Gastroretentive Drug Delivery (GRDDS). It is based upon the osmotically controlled release mechanism which offers a sustained therapeutic action while reducing the side effects. Various drugs with a shorter half-life and a small absorption window get highly benefited By FODDS. FODDS also finds a unique place among the other GRDDS by surpassing their performance. FODDS incorporates a variety of ingredients such as osmotic agents, semi permeable substance, gas generating Agent and a gel forming agent. The preparation of the system involves techniques like direct compression and coating process. Characterisation studies like in-vitro dissolution study, in-vivo radiological study and pharmacokinetic study were adapted for evaluation of FODDS. Many studies have been carried out to illustrate the efficiency of the FODDS in overcoming the drawbacks such as poor bioavailability, drug wastage etc. Active agents derived from the field of pharmacognosy have also been benefited by FODDS since they prevent the enzymatic degradation of the active agents and and improve their bioavailability. FODDS also provides a robust pharmacokinetic profile with both in-vitro and in-vivo drug release rate which results in excellent in-vitro/in-vivo correlation due to its controlled release mechanism. This review is primarily focused on providing an overall insight into FODDS while giving detailed information regarding its design, development, mechanism, characterisation and a precise overview of various studies carried out using FODDS.Keywords
Drug Delivery System, Intragastric System, Gastro Retentive, Floating Osmotic System, Controlled Drug Delivery.References
- Ratnaparkhi M. P and Gupta J. P. Sustained-release oral drug delivery system - an overview. International Journal of pharmacy review and research. 2013; 2(3): 11- 21.
- Khatri N , Nikam S and Bilandi A . Oral osmotic drug delivery system: a review. International Journal of Pharmaceutical sciences and research. 2016; 7(6): 2302-2312.
- Rastogi S.K, Vaya N, and Mishra B. Osmotic pump: a novel concept in rate controlled oral drug delivery. Eastern Pharmacist 1995; 38:79–82.
- Keraliya R.A et al., Osmotic drug delivery systems a part of modified release dosage form. ISRN Pharmaceutics 2012; 2012:528079
- Reddy P. D and Swarnalatha D. Recent advances in novel drug delivery systems. International Journal of PharmTech Research, 2010; 2(3):2025–2027.
- Gupta P.B, Thakur N, Jain N.P. Osmotically Controlled Drug Delivery System with Associated Drugs. Journal of pharmacy and pharmaceutical sciences. 2010; 13(3): 571-580.
- Pawar V. K et al ., Gastroretentive dosage forms: A review with special emphasis on floating drug delivery systems. Drug Delivery. 2011; 18(2): 97–110
- Khan ZA, Tripathi R, Mishra B. Floating elementary osmotic pump tablet (FEOPT) for controlled delivery of diethylcarbamazine citrate: a water-soluble drug. American association of pharmaceutical scientists.2011; 12(4):1312-23.
- Davis SS, Hardy JG, Far JW. Transit of pharmaceutical dosage forms through the small intestine. Gut. 1986; 27:886–92.
- Bardonnet PL et al., Gastroretentive dosage forms: overview and special case of Helicobacter pylori. Journal of Control Release. 2006; 111:1 –18.
- Desai S, Bolton S. A floating controlled-release drug delivery systems: in vitro–in vivo evaluation. Pharmaceutical Research. 1993; 10:1321-1325.
- Guan J et al., A novel gastric-resident osmotic pump tablet: In vitro and in vivo evaluation. International Journal of Pharmaceutics. 2010; 383:30–36.
- Chueh H.R, Zia H, Rhodes C.T. Optimization of sotalol floating and bioadhesive extended-release tablet formulations. Drug Development and Industrial Pharmacy. 1995; 21:1725–1747.
- Iannuccelli V et al., Air compartment multiple-unit system for prolonged gastric residence. Part I. Formulation study. International Journal of Pharmaceutics. 1998; 174:47–54.
- Arora S et al., Floating Drug Delivery Systems: A Review. American association of pharmaceutical scientists. 2005; 6 (3): 47.
- Kumar P, Singh S, Mishra B. Floating osmotic drug delivery system of ranitidine hydrochloride: development and evaluation— a technical note. American association of pharmaceutical scientists. 2008; 9:480–5.
- Chien Y.W. Novel drug delivery systems, Second edition.Taylor and Francis. Boca Rosa.1993
- Michaels A.S; Drug delivery device with self-activated mechanism for retaining device in selected area. U.S. Patent 3,786,813, 1974
- Mehta B.P, Doshi A.M, Joshi M.D. Floating osmotic device for controlled release drug delivery. United States Patent Application Publication. US 20030064101A1, 2003.
- Falk et al., An oral formulation for gastric antibacterial treatment as well as a process thereof and the use. PCT Publication No. WO94/00112, 1994.
- Verma R.K, Mishra B and Garg S. Osmotically Controlled Oral Drug Delivery. Drug Development and Industrial Pharmacy. 2000; 26(7):695-708.
- N. Mazerne et al., Intragastric behavior and absorption kinetics of a normal and ‘floating’ modified-release capsule of Isradipine under fasted and fed conditions. 1988. Journal of Pharmaceutical Sciences. 77(8):647–657.
- Theeuwes F et al., Osmotic delivery systems for the β-adrenoceptor antagonists metoprolol and oxprenolol, design and evaluation of systems for once-daily administration. British Journal of Clinical Pharmacology. 1985; 19:69S–76S.
- Gupta S. K., Atkinson L., Theeuwes F, Wong P., Longstreth J. Pharmacokinetics of verapamil from an osmotic system with delayed onset. European Journal of Pharmacy and Biopharmaceutics. 1996; 42:74–81.
- Chao S. T et al., Effect of food on bioavailability of pseudoephedrine and brompheniramine administered from a gastrointestinal therapeutic system Journal of Pharmaceutical Sciences. 1991; 80: 432–435.
- Swanson DR et al., Nifedipine gastrointestinal therapeutic system. Am J Med 1987; 83 Suppl. 6B: 3–9
- Kuczynski et al., One approach for delivering pharmaceutical agents that are insoluble in aqueous solvents. U.S. Pat. No. 5,545,413.
- W.A. Ritschel W A, Menon A, Sakr A. Biopharmaceutic evaluation of furosemide as a potential candidate for a modified release peroral dosage form, Methods and Findings in Experimental and Clinical Pharmacology. 1991; (13):629–636.
- Blaser M J. Hypotheses on the pathogenesis and natural history of Helicobacter pylori-induced inflammation. Gastroenterology. 1992; 102:720–727.
- C.G. Wilson, N. Washington. The stomach: its role in oral drug delivery, in M.H. Rubinstein (Ed.). Physiological Pharmaceutics: Biological Barriers to Drug Absorption. Ellis Horwood, Chichester. 1989; 47–70.
- Deshpande A.A et al., Controlled-release drug delivery systems for prolonged gastric residence: an overview, Drug Development and Industrial Pharmacy.1996; 22:531–539.
- Haring N, Salama Z, Jaeger H. Triple stage quadropole mass spectrometric determination of bromocriptine in human plasma with negative ion chemical ionization, Arzneim. Forsch. 1988; 38:1529–1532.
- Rouge N, Buri P and Doelker E. Drug absorption sites in the gastrointestinal tract and dosage forms for site-specific delivery. International Journal of Pharmaceutics. 1996; 136:117–139.
- Singla D, Hari Kumar SL and Nirmala. Osmotic pump drug delivery- a novel approach. International journal of research in pharmacy and chemistry. 2012; 2(2):661-670.
- McClelland GA et al., The solubility modulated osmotic pump: In vitro/ in vivo release of diltiazem HCl, Pharmaceutical Research. 1991; 8:88-92
- Bauer K, Kaik G and Kaik B. Osmotic-release oral drug delivery system of metoprolol in hypertensive asthmatic patients. Pharmacodynamic effects on beta 2-adrenergic receptors, Hypertension. 1994; 24:339-346
- Rudnic EM et al., Osmotic drug delivery system. US Patent 6110498; 2000.
- Thombre AG, DeNoto AR and Gibbes DG. Delivery of glipizide from asymmetric membrane capsules using encapsulated excipients, Journal of Controlled Release. 1999; 60:333-341
- Tripathi P et al., Floating drug delivery system. International Journal of Reearch and Development in Pharmacy and Life Sciences. 2012; 1(1):1-10.
- Li S et al., Statistical optimization of gastric floating system for oral controlled delivery of calcium. American Association of Pharmaceutical Scientists. 2001; 2(1):1.
- Talukder R and Fassihi R. Gastroretentive Delivery Systems: A mini Review. Drug Development and Industrial Pharmacy. 2004; 30(10):1019-1028.
- Hejazi R and Amiji N. Stomach specific anti H.Pylori therapy. I: Preparation and characterization of tetracycline of a floating multiple unit capsule, a high density loaded chitosan microspheres. International Journal of Pharmaceutics. 2002; 235:87-94.
- Cooerman M P, Krausgrill P and Hengels K J. Local gastric and serum amoxicillin concentration after different oral application forms. Antimicrobial Agents and Chemotherapy. 1993; 37:1506-1509.
- Dave B S, Amin A F and Patel M. Gastroretentive drug delivery system of Ranitidine HCl formulation and in vitro evaluation. ; American Association of Pharmaceutical Scientists. 2004; 5:1-10.
- Sawicki W. Pharmacokinetics of verapamil and norverapamil from controlled release floating pellets in humans. European Journal of Pharmaceutics and Biopharmaceutics. 2002; 53:29-35.
- Singh B M and Kim K H. Floating drug delivery systems: an approach to oral controlled drug delivery via gastric retention. Journal of Controlled Release. 2000; 63:235-259.
- Jain S K, Agarwal G P, Jain N K. Evaluation of porous carrier based floating orlistat microspheres for gastric delivery. American Association of Pharmaceutical Scientists. 2006; 7(4):90.
- Sriamornsak P, Thirawong N, Puttipipatkhachorn S. Morphology and buoyancy of oil entrapped calcium pectinate gel beads. American Association of Pharmaceutical Scientists. 2004; 6(3):24.
- Patil J M et al., Trends in floating drug delivery systems. Journal of scientific and industrial research. 2006; 65:11-21.
- Garg R, Gupta GD. Progress in Controlled Gastroretentive Delivery Systems. Tropical Journal of Pharmaceutical Research. 2008; 7(3):1055-1066.
- Eckenhoff B, Theeuwes F and Urquhart J. Osmotically actuated dosage forms for rate-controlled drug delivery. Pharmaceutical Technology. 1987; 11:96–105.
- Jensen JL et al.,Variables that affect the mechanism of drug release from osmotic pumps coated with acrylate/methacrylate copolymer latexes. Journal of Pharmaceutical Sciences. 1995; 84(5):530-533.
- Sastry S, Phanidhar K, Brian B. Osmotic controlled drug delivery system, in Li Xiaoling, Jasti Bhaskara R (eds). Design of Controlled Release Drug Delivery Systems. McGraw-Hill Companies, INC, New York. 2006; 203-229.
- Avinash Y et al., Role of excipients and polymeric advancements in preparation of floating drug delivery systems. International Journal of Pharmaceutical Investigation. 2015 ; 5(1):1–12.
- Rania A, Ishak H. Buoyancy-Generating Agents for Stomach-specific Drug Delivery: An Overview with Special Emphasis on Floating Behavior. Journal of Pharmacy and Pharmaceutical Sciences. 2015; 18(1):77 – 100.
- Rabadia N et al., The floating drug delivery system and it's impact on calcium channel blocker: A review article. Journal of pharmaceutical Science and Technology. 2012; 4:835–67.
- Shah SH, Patel JK and Patel NV. Stomach specific floating drug delivery system: A review. International Journal of Pharmtech Research. 2009; 1:623–33.
- Ozdemir N and Sahin J. Design of a controlled release osmotic pump system of ibuprofen. International Journal of Pharmaceutics. 1997; 158:91–97.
- Krishnaiaha Y. S. R. et al., Studies on development of oral colon targeted drug delivery systems for metronidazole in treatment of amoebiasis. International Journal of Pharmaceutics. 2002; 236:43–55.
- Bandameedi R and Pandiyan S. Formulation and Evaluation of Floating Osmotic Tablets of Nizatidine. Journal of Applied Pharmaceutical sciences. 2015; 8:1.
- Narang N, An updated review on floating drug delivery system. International Journal of applied pharmaceutical science. 2011; 3(1):17.
- R. K. Verma and S. Garg. Development and evaluation of osmotically controlled oral drug delivery systems of glipizide, European Journal of Pharmaceutics and Biopharmaceutics. 2004; 57:513–525.
- Srivastava A K. Oral sustained delivery of Atenolol from floating matrix tablets—formulation and in-vitro evaluation. Drug Development and Industrial Pharmacy 2005; 31:367–374.
- Freidman M and Hoffman A. Furosemide pharmacokinetics and pharmacodynamics following gastro-retentive dosage form administration to healthy volunteers. Journal of Clinical Pharmacology. 2003; 43: 711‐720
- Rosen Y, Gurman P, Elman N M .Drug Delivery An Integrated Clinical and Engineering Approach. New York. 2017.
- Klausner E et al., Novel Gastroretentive Dosage Forms: Evaluation of Gastroretentivity and Its Effect on Levodopa Absorption in Humans. Pharmaceutical research. 2003; 20(9):1466–73.
- Dorożyński P et al., Development of a system for simultaneous dissolution studies and magnetic resonance imaging of water transport in hydrodynamically balanced systems: A technical note. American Association of Pharmaceutical Scientists. 2007; 8(1):E109–E12.
- Goole J et al. Pharmacoscintigraphic and pharmacokinetic evaluation on healthy human volunteers of sustained-release floating minitablets containing levodopa and carbidopa. International Journal of Pharmaceutics. 2008; 364(1):54–6.
- Klausner EA et al., Novel levodopa gastro-retentive dosage form: In-vivo evaluation in dogs. Journal of Controlled Release.2003; 88(1):117–26.
- Sanja S et al., Development and Evaluation of Novel Floating Osmotic Capsule for Zero-Order Delivery of Andrographis Paniculata Extract. American Journal of PharmTech Research. 2014; 4(6).
- Fang Y, Shi QW. Studies on preparation and dissolution test in vitro of intragastric floating two-chamber osmotic pump tablets of total alkaloids of Coptis chinensis and Evodia rutaecarpa. Zhong Yao Cai. 2011; 34(5):779-82.
- Fang Y, Pan ZH, Cao DY. Study on Preparation and Pharmacokinetics of Irbesartan Intragastric Floating Osmotic Pump Tablets in Dogs. China Pharmacy. 2013; 01.
- Zhang Z et al., Design and Evaluation of a Novel Floating Osmotic Pump System. Journal of Pharmaceutical Sciences. 2009; 12(1): 129 – 137.
- Zhao F et al., Optimization of a floating osmotic pump system of ambroxol hydrochloride using central composite design-response surface methodology and its pharmacokinetics in Beagle dogs. Yao Xue Xue Bao. 2011; 46(12):1507-14.
- Zhang Z et al., Optimization of a floating osmotic pump system of dipyridamole using central composite design-response surface methodology. Yao xue xue bao. 2009; 44:203-7.
- Manvendra S et al., Osmotically Regulated Floating Asymmetric Membrane Capsule for Controlled Site-Specific Delivery of Ranitidine Hydrochloride: Optimization by Central Composite Design. American Association of Pharmaceutical Scientists. 2012; 13(4).
- Kamble M S et al., Optimization Of Floating Osmotic Drug Delivery System Of Diltiazem Hydrochloride Using 32 Factorial Design. Indo American Journal of Pharmaceutical Research. 2013; 3(6):4585-4593.
- Patel M et al., Osmotically regulated floating capsule for controlled delivery of acyclovir: a water-soluble drug. International research journal of pharmacy. 2017, 8 (9).
- Vivek K Pawar, Shaswat Kansal, Shalini Asthana and Manish K Chourasia. Industrial perspective of gastroretentive drug delivery systems: Physicochemical, biopharmaceutical, technological and regulatory consideration. Expert Opinion on Drug Delivery. 2012; 9(5).
- Available from : https://www.drugs.com/availability/generic-coreg-cr.html.