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Debnath, Subhashis
- Preparation and Evaluation of Solid Dispersion of Terbinafine Hydrochloride
Abstract Views :454 |
PDF Views:2
Authors
Affiliations
1 Seven Hills College of Pharmacy, Tirupati-517561, Andhra Pradesh, IN
2 Vikas Institute of Pharmaceutical Sciences, Andhra Pradesh, IN
3 Jawaharlal Nehru Technological University, Anantapur, Andhra Pradesh, IN
1 Seven Hills College of Pharmacy, Tirupati-517561, Andhra Pradesh, IN
2 Vikas Institute of Pharmaceutical Sciences, Andhra Pradesh, IN
3 Jawaharlal Nehru Technological University, Anantapur, Andhra Pradesh, IN
Source
Asian Journal of Pharmacy and Technology, Vol 3, No 1 (2013), Pagination: 9-15Abstract
Terbinafine hydrochloride is a synthetic antifungal drug. It is slightly soluble in water (3mg/ml) and having high permeability through stomach. This results in poor bioavailability after oral administration. Therefore solid dispersion of terbinafine HCl with polyethylene glycol-6000 (PEG 6000) and mannitol were prepared with a view to increase its water solubility. In this study solid dispersion of the drug were prepared by melting method and the drug was taken with carrier in the proportions of (1:1, 1:2 and 1:3). The rate of dissolution of terbinafine HCl was increased with the proportion of (1:3) (Drug: PEG 6000) when compared to the other formulations. In order to predict and correlate the release behavior of the drug from the polymer matrix the dissolution data were fitted in to a suitable model to describe the drug release behavior from polymeric system. The surface morphology of the prepared solid dispersion and drug alone were examined by SEM analysis. The SEM result shows that in the case of solid dispersion of terbinafine HCl, particles were in almost amorphous form, which indicates a reduction in particle size.Keywords
Antifungal, Bioavailability, Solid Dispersion, Polymer Matrix, SEM
References
- Betageri GV and Makarla KR . Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques. Int. J. Pharm. 126(1);1995:155-160.
- Breitenbach J, Schrof W and Neumann J . Confocal Ramanspectroscopy: analytical approach to solid dispersions and mapping of drugs. Pharm. Res.16(7);1999:1109-1113.
- Chiou WL and Riegelman S. Preparation anddissolution characteristics of several fast-release soliddispersions of griseofulvin. J. Pharm. Sci.58(12);1969:1505-1510.
- Ho HO, Shu HL, Tsai T and Sheu MT. The preparation and characterization of solid dispersions on pellets using a fluidized bed system. Int. J. Pharm.139;1996: 223-229.
- Lloyd GR, Craig DQ and Smith A. An investigation into the melting behavior of binary mixes and solid dispersions of paracetamol and PEG 4000. J.Pharm. Sci.86(9);1997: 991-996.
- Morris KR, Knipp GT and Serajuddin ATM. Structural properties of poly (ethylene glycol)-polysorbate 80 mixture, a solid dispersion vehicle. J.Pharm. Sci.81(2);1992:1185-1188.
- Moneghini M, Kikic I, Voinovich D and Perissutti B. Processing of carbamazepine-PEG 4000 solid dispersions with supercritical carbon dioxide: preparation, characterization, and in vitro dissolution.Int. J. Pharm.222(1);2001: 129-138.
- Batra V, Shirolkar V.S, Mahaparaie P.R, Solubility and dissolution enhancement of Glipizide by solid dispersion technique.Int.J.Pharm.42(4); 2008:1:373-378 .
- Vanshiv S.D, Rao M.R.P, Sonar G.S, Physicochemical characterization and invitro dissolution of Domperidene by solid dispersion technique. Int.J.Pharm.43(1);2009: 1:86-90.
- Bada pragati kumar, Rama Krishna Reddy M, Enhancing in vitro bioavailability of Nevirapine by employing solid dispersion technique. J.Chem. and Pharm. Sci. 4(1);2011:86-92.
- Meka lingam, Vobalaboina venkateswarlu, Enhancement of solubility and dissolution rate of poorly water soluble drug using co-solvency and solid dispersion techniques. Int.J. Pharm. Sci and Nano Tech.l.1(1);2009: 349-356.
- Bhawandeep gill, Tejvir kaur, Sandeep kumar, Formulation and evaluation of Glimepiride solid dispersion tablets. Assn. J. Pharmaceutics.1(4); 2010:212-218.
- Rajesh Kumar Maheshwari, Arpna Indurkhta, Novel application of mixed hydrotropic solubilization technique in the formulation and evaluation of hydrotropic solid dispersion of Aceclofenac. Assn.J.Pharmaceutics.1(4);2010:235-238.
- Bourne DWA. Pharmacokinetics. In: Banker GS, Rhodes CT, Modern Pharmaceutics, 4th ed., Marcel Dekker Inc., New York.2002.
- Lordi NG . Sustained release dosage form. In: The Theory and Practice of Industrial Pharmacy, 3rd Ed., Lea and Febiger, Philadelphia, USA.1986
- Cox PJ, Khan KA, Munday DL and Sujja-areevath J. Development and evaluation of a multiple-unit oralsustained release dosage form for S (+)-ibuprofen: preparation and release kinetics. Int.J. Pharm.193(2);1999: 73-84.
- Siepmann J, Kranz H, Peppas NA and Bodmeier R. Calculation of the required size and shape of hydroxypropylmethylcellulose matrices to achieve desired drug release profiles. Int. J. Pharm. 201 (3);2000: 151-164.
- Siepmann J, Kranz H, Bodmeier R and Peppas NA .HPMCmatrices for controlled drug delivery: a new model combining diffusion, swelling and dissolution mechanisms and predicting the release kinetics. Pharm. Res.16(4);1999: 1748-1756.
- Formulation and Evaluation of Herbal Antimicrobial Deodorant Stick
Abstract Views :171 |
PDF Views:0
Authors
Affiliations
1 Seven Hills College of Pharmacy, Tirupati, IN
1 Seven Hills College of Pharmacy, Tirupati, IN
Source
Research Journal of Topical and Cosmetic Sciences, Vol 2, No 1 (2011), Pagination: 21-24Abstract
Deodorants are chemicals that prevent or reduce axillary malodor, which results from bacterial breakdown of perspiration from eccrine and apocrine sweat glands. The sweaty odor is caused by the interaction between a variety of substances including low-molecular-weight fatty acids (i.e caproic, caprylic, isovaleric, butyric), lactates, urea and ammonia, cholesterol, and other steroid compounds. Odor control can be achieved by various means - basic hygiene (washing with soap and water) is the most important but also by antimicrobial agents, antiperspirant, fragrances or any combination of these. Here deodorant sticks were prepared with herbal antimicrobial agent and the sticks were characterized for pH, softening point, disintegration time, colour loss, stability upon 2 weeks storage and anti microbial test. The physicochemical properties remain unchanged after 2 weeks storage. The result of anti microbial activity shows that all the formulations have antibacterial activity towards all tested phytopathogenic bacteria.Keywords
Deodorant, Sweat, Odour, Stability, Pathogen.- Radiopharmaceuticals and their Therapeutic Applications in Health Care System
Abstract Views :205 |
PDF Views:2
Authors
Affiliations
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Tirupati–517561, Andhra Pradesh, IN
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Tirupati–517561, Andhra Pradesh, IN
Source
Asian Journal of Research in Pharmaceutical Sciences, Vol 5, No 4 (2015), Pagination: 221-226Abstract
Radiopharmaceuticals, as the name suggests, are pharmaceutical formulations consisting of radioactive substances (radioisotopes and molecules labelled with radioisotopes), which are intended for use either in diagnosis or therapy or diagnosis. Recently, however, there has been a significant growth of this branch of nuclear medicine with the introduction of a number of new radionuclides and radiopharmaceuticals for the treatment of metastatic bone pain, neuroendocrine and other tumours. This review focused on the production of radiopharmaceuticals, their applications, labelling, packaging and storage.Keywords
Radiopharmaceuticals, Radioactive, Nuclear Medicine.- Food as a Vaccine
Abstract Views :176 |
PDF Views:0
Authors
Affiliations
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati, IN
2 Department of Pharmaceutical Chemistry, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati, IN
3 Department of Pharmacology, Sri Padmavathi School of Pharmacy, Tiruchanoor, Tirupati, IN
4 Department of Pharmaceutical Analysis, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati, IN
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati, IN
2 Department of Pharmaceutical Chemistry, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati, IN
3 Department of Pharmacology, Sri Padmavathi School of Pharmacy, Tiruchanoor, Tirupati, IN
4 Department of Pharmaceutical Analysis, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati, IN
Source
Research Journal of Pharmaceutical Dosage Form and Technology, Vol 7, No 2 (2015), Pagination: 161-165Abstract
As the science and technology advances, a leap in medical field occurred and all the painful vaccination procedures replaced with modernized techniques like edible vaccines, a non-invasive technique. Vaccine contains weak pathogens of bacteria or virus or a killed bacterial suspension or toxins produced by bacterial strains, when taken inside human body, our immune system finds out the foreign particle and it produces a group of antibodies to eradicate it and making a memory of it. Edible vaccines are genetically modified crop, in which vaccines are produced in the plant parts when antigenic proteins are transgenically introduced into edible crop and work same as that of original vaccines. Present review is focused on several methods used in production of edible vaccines and the types of food used for production of edible vaccines. And the challenges we are still facing in development which needs to be focused more by the future generations.Keywords
Edible Vaccine, Transgenic Plant, Immunity, Potato, Tomato.- Chronopharmaceutics as a Novel Approach for Clinically Relevant Drug Delivery System
Abstract Views :215 |
PDF Views:0
Authors
Affiliations
1 Seven Hills College of Pharmacy, Tirupati, 517 561, A.P., IN
2 Vikas Institute of Pharmaceutical Sciences, Andhra Pradesh, IN
1 Seven Hills College of Pharmacy, Tirupati, 517 561, A.P., IN
2 Vikas Institute of Pharmaceutical Sciences, Andhra Pradesh, IN
Source
Research Journal of Pharmaceutical Dosage Form and Technology, Vol 4, No 6 (2012), Pagination: 309-317Abstract
Chronopharmaceutics has been described as a branch of pharmaceutics devoted to the design and evaluation of drug delivery system that release a bioactive agent at a rhythm that ideally matches the biological requirement of a given drug therapy. The circadian clock acts like a multifunction timer to regulate homeostatic systems such as sleep and activity, hormone levels, appetite, and other bodily functions with 24h cycles. Diseases such as hypertension, asthma, peptic ulcer, arthritis, etc, follow the body's circadian rhythm. The goal in drug delivery research is to develop formulations to meet therapeutic needs relating to particular pathological conditions. Research in the chronopharmacological field has demonstrated the importance of biological rhythm in drug therapy, and this has brought a new approach to the drug delivery systems. The application of biological rhythm to pharmacotherapy may be correlated by the appropriate timing of dosing of these drug delivery systems to synchronize drug concentrations to rhythms in disease state.Keywords
Chronopharmaceutics, Bioactive Agent, Circadian Clock, Circadian Rhythm, Chronopharmacological, Pharmacotherapy.- Formulation and Evaluation of Liquid Soap Containing Herbal Antimicrobial Agent
Abstract Views :159 |
PDF Views:0
Authors
Subhashis Debnath
1,
M. Niranjan Babu
1,
Mahesh Dega
1,
K. Bharathi
1,
T. Jyothsna
1,
D. Revathi
1,
T. S. Kishore Kumar
1
Affiliations
1 Seven Hills College of Pharmacy, Tirupati-517561, Andhra Pradesh, IN
1 Seven Hills College of Pharmacy, Tirupati-517561, Andhra Pradesh, IN
Source
Research Journal of Pharmacognosy and Phytochemistry, Vol 3, No 5 (2011), Pagination: 225-231Abstract
Hand washing for hand hygiene is the art of cleaning the hands with or without the use of water or another liquid, or with the use of soap, for the purpose of removing soil, dirt, and/or microorganisms. The main medical purpose of washing hands is to cleanse the hands from pathogens (including bacteria or viruses) and chemicals which can cause personal harm or disease. This is especially important for people who handle food or work in the medical field, but it is also an important practice for the general public. In response to this concern, we formulated the antibacterial Liquid soap. Experiment was performed by selecting the herbs which were reported to have antibacterial activity. They are Ocimum sanctum and Eugena caryophyllus. Formulated liquid soaps were evaluated for physical parameters like colour, fragrance and chemical parameters like pH, % Free alkali, Test for chlorides, Foam height, Foam retention, Alcohol insoluble matter, Microbial count etc. and the obtained results were in the acceptable limits except foam height and foam retention as we are not using SLS.
Keywords
Liquid Soap, Infection, Antibacterial, Free Alkali, Microbial Count.- Formulation and Evaluation of Multipurpose Herbal Wash
Abstract Views :209 |
PDF Views:1
Authors
Affiliations
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati-517561, IN
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Venkatramapuram, Tirupati-517561, IN
Source
Research Journal of Topical and Cosmetic Sciences, Vol 4, No 2 (2013), Pagination: 48-53Abstract
Personal hygiene is the process of maintaining cleanliness. Failure to maintain adequate personal hygiene can result in illnesses of all kinds. Poor hand-washing practices increase the likelihood of contracting contagious illnesses such as influenza and food-borne illnesses like Salmonella infection. Multipurpose herbal wash is expected to be proven more economical compared to conventional products as the customer may get the desired effect by buying one container of bodywash which can act as a shampoo also. Formulated herbal wash preparations were evaluated for physical parameters like colour, fragrance and chemical parameters like pH, percent of solids contents, viscosity, surface tension, dirt dispersion, cleaning action, foaming ability and foam stability, antimicrobial activity, anti fungal activity and results shown that all were in the accepted limits. Combination of neem and tulsi was found to be effective, easier to produce stable herbal wash formulation. It is having good foaming characters and anti bacterial as well as anti fungal activity. So it can be suitable for both skin and hair care compared to other synthetic preparations.Keywords
Personal Hygiene, Multipurpose Herbal Wash, Antimicrobial, Antifungal.- Polymers used in the Designing of Controlled Drug Delivery System
Abstract Views :138 |
PDF Views:3
Authors
Affiliations
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Tirupati-517561, A.P., IN
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Tirupati-517561, A.P., IN
Source
Research Journal of Pharmacy and Technology, Vol 10, No 3 (2017), Pagination: 903-912Abstract
Polymers are becoming very important in the drug delivery field. To control the drug release rate from the formulation, polymers are being used as the main tool. Polymers can be used as taste masking agents, to enhance stability of drug and to modify drug release characteristics. Biodegradable materials are used in medicine and other areas. In recent years there has been increase in use of biodegradable polymers. Biodegradable polymers are of two classes; synthetic and natural polymers. Natural polymers offer few advantages than synthetic polymers. Although polymers are used extensively as pharmaceutical packaging, this review is concerned with the use of polymers in the formulation of various dosage forms.Keywords
Polymers, Drug Delivery System, Controlled Drug Delivery, Biodegradable Polymers, Drug Release Mechanism.- Formulation and Development of a Compression Coated, Matrix Based, Tablet of Verapamil HCl using Design of Experiments
Abstract Views :194 |
PDF Views:0
Authors
Affiliations
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Tirupati-517561, A.P, IN
2 Department of Pharmaceutics, J S S College of Pharmacy, Ooty-643001, A.P, IN
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Tirupati-517561, A.P, IN
2 Department of Pharmaceutics, J S S College of Pharmacy, Ooty-643001, A.P, IN
Source
Asian Journal of Pharmacy and Technology, Vol 7, No 3 (2017), Pagination: 117-126Abstract
Compression coating provides a unique platform for formulating modified release products in a way the dosage form can successfully be targeted to localize the release of the drug in any desired portion of the GIT without the additional step of film coating. The current work focuses on the development and optimization of modified release Verapamil Hydrochloride tablets using compression coating. The effect of various concentrations of different grades HPMC polymers, like, K4M, K15M and K100M on the release profile was studied in DOE environment. The results of the DOE provide an optimized range of the three polymers which could potentially give the targeted release profile for all drugs which have solubility profiles similar to Verapamil HCl. Three batches of optimized formulation were loaded on to accelerated stability studies at 40° C/75% RH in HDPE containers and the 3 months stability data indicates that there is no significant change in either the potency of the dosage form or its in vitro dissolution profile.Keywords
Verapamil, DOE, HPMC, Formulation.References
- Yeswanth Reddy Musukula: Design and Evaluation of Compression Coated Colon Targeted Tablets of Ketorolac Tromethamine by Using Natural Polymers and Their Combination with Hpmc K100m.Int. J Rese in Pharm Nano Sci.2014;3:408-417.
- Patel Rushikesh Chandubhai, Sindhu Abraham, Srinivasan Bharath, Varadharajan Madhavan: Compression coated tablets of Flurbiprofen- A chronotherapeutic approach. J Sci. Innov Res.2013;2:914-926.
- Ray Brijesh, M.M. Gupta: Formulation and Evaluation of Once Daily Sustained Release Matrix Tablet of Verapamil Hydrochloride. J Drug Deli Thera.2013;3:55-58
- Margret Chandira, Mehul, Debjit, Chiranjib, Kumudhavalli, B. Jayakar formulation, Design and Development of Buccoadheshive Tablets of Verapamil Hydrochloride. Int. J Pharm Res.2009;1:1663-1677.
- Birajdar Shivprasad M., Bhusnure Omprakash G, Mulaje Suraj S: Formulation and Evaluation of Fast Disintegrating Losartan Potassium Tablets by Formal Experimental Design. Int J Res Deve Pharma Life Sci.2014; 3:1136-1150.
- Nandini. D. Banerjee, Sushma R: Formulation and Evaluation of Compression Coated Tablets of Cefpodoxime Proxetil. Inter J Pharma Sci. Rese.2013;7:104-112.
- SS. Khadabadi, Nahid H. Chishti, Farhan M. Khan, Akeel A. Tadvee: Formulation and Evaluation of Press Coated Tablet of Ketoprofen – A Chronotherapeutic Approach. Inter J Pharm Pharmac Sci.2013;5:733-740.
- Parag A. Kulkarni, Mahendra Jaiswal, Santosh B. Jawale, Satish V. Shirolkar, Pramod V. Kasture: Development and Evaluation of Press Coated Tablets for Chronopharmaceutical Drug Delivery Using Gellable and Permeable Polymers. Scho Res Lib. 2010;2:482-497.
- A Review on Buccal Drug Delivery System
Abstract Views :279 |
PDF Views:0
Authors
Affiliations
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Venkataramapuram, Tirupati- 517561, Andhra Pradesh, IN
1 Department of Pharmaceutics, Seven Hills College of Pharmacy, Venkataramapuram, Tirupati- 517561, Andhra Pradesh, IN
Source
Research Journal of Pharmaceutical Dosage Form and Technology, Vol 9, No 3 (2017), Pagination: 109-113Abstract
Bio adhesion can be defined as a phenomenon of interfacial molecular attractive forces in the midst of the surfaces of biological substrate and the natural or synthetic polymers, which allows the polymer to adhere to biological surface for an extended period of time. Within the oral mucosal cavity, the buccal region offers an adorable route of administration for systemic drug delivery. The buccal mucosa is considered to be a promising site for the systemic delivery of drugs where a rapid onset of action is required and for drugs that are not easily administered via other routes than by injection. The buccal mucosa being a highly vascularised area helps in rapid systemic absorption of the drug, thereby avoiding hepatic “first-pass effect” of drugs leading to quicker onset of action, which could be especially important in the management of crisis situations like cardiac arrest, epileptic seizures, severe nausea and vomiting. This article aims at reviewing on buccal drug delivery system which includes the mechanism and factors affecting buccal absorption and the methods to increase drug delivery via buccal route.Keywords
Bioadhesion, Buccal Mucosa, First-Pass Effect, Cardiac Arrest, Epileptic Seizures.References
- Joseph A. DiMasi et al., The price of innovation: new estimates of drug development costs, Journal of Health Economics 2003; 22: 151-185.
- Mathias N.R. and Hussain A.M, Non-invasive systemic drug delivery: developability considerations for alternate routes of administration, J. Pharm. Sci. 2010; 99:1-20.
- S. Yajaman et al., Buccal bioadhesive drug delivery – A promising option for orally less efficient drugs, J Control Release 2006; 114: 15-40.
- Dixit R.P and Puthli S.P., Oral strip technology: Overview and future potential, J Control Release 2009; 139: 94-107.
- Lee Jin W. et al., Bioadhesive-based dosage forms: the next generation, J. Pharm. Sci. 2000; 89:850-866.
- Colonna Claudia, Innovative drug delivery systems for challenging molecules, Scientifica Acta 2007; 1(1): 70-77.
- Andrews Gavin P. et al., Mucoadhesive polymeric platforms for controlled drug delivery, Eur J Pharm Biopharm 2009; 71:505518.
- Khairnar G.A. and Sayyad F.J., Development of buccal drug delivery system based on mucoadhesive polymer, International Journal of Pharm Tech Research 2010; 2(1): 719-735.
- Madhav N.V. Satheesh et al., Orotransmucosal drug delivery systems: A review, J Control Release 2009; 140: 2-11.
- Vyas S.P. and Khar R.K., Controlled drug delivery-concepts and advances. Vallabh Prakashan, first edition, New Delhi, 2002.
- Bhalodia Ravi et al., Buccoadhesive drug delivery Systems: A review, International Journal of Pharma and Bio Sciences 2010; 1(2): 1-32.
- Obradovic T. and Hidalgo Ismael J., DRUG ABSORPTION Studies Biotechnology: Pharmaceutical Aspects, AAPS Press, Vol.7 (2), 2008: 167-181.
- Junginger H.E. et al., Recent advances in buccal drug delivery and absorption- in vitro and in vivo studies, J Control Release 1999; 149: 149-159.
- Rossi Silvia et al., Buccal drug delivery: A challenge already won?, Drug Discov Today Technol 2005; 2(1): 59-65.
- Miller N.S. et al., The use of mucoadhesive polymers in buccal drug delivery, Adv Drug Deliv Rev 2005; 57:1666-1691.
- Gandhi SD, Pandya PR, Umbarkar R, Tambawala T and Shah MA- Mucoadhesive drug delivery system- an unusual maneuver for site specific drug delivery system, Inter. J. Pharm. Sci., 2011, 851- 872.
- Patil SB, Murthy RSR, Mahajan HS, Wagh RD and Gattani SGMucoadhesive polymers: means of improving drug delivery, Pharm. Times, 2006, 38 (4), 25-28.
- Overview on Buccal Drug Delivery Systems, N. G. Raghavendra Rao, B. Shravani- Mettu Srikanth Reddy, J. Pharm. Sci. & Res. Vol.5(4), 2013, 80 – 88.
- Sevda Senel, Mary Kremer, Katalin Nagy and Christopher SquierDelivery of Bioactive Peptides and Proteins Across Oral (Buccal) Mucosa, Current Pharmaceutical Biotechnology, 2001; 2: 175-186.
- Amir H, et al, Systemic drug delivery via the buccal mucosal route, Pharmaceutical technology, 2001, 1-27. 4.
- Pramod Kumar TM et al, Oral transmucosal drug delivery systems, Indian drug, 2004, 41(2), 63-1.
- Sudhakar Y, Knotsu K, Bandopadhyay AK. Bio adhesive drug delivery – A promising option for orally less efficient drugs. J Control Rel 2006;114:15-40.
- Coronavirus Disease (COVID-19): A Global Threat
Abstract Views :150 |
PDF Views:0
Authors
Affiliations
1 Royal School of Pharmacy, The Assam Royal Global University, Guwahati, Assam, IN
1 Royal School of Pharmacy, The Assam Royal Global University, Guwahati, Assam, IN
Source
Asian Journal of Pharmacy and Technology, Vol 12, No 1 (2022), Pagination: 63-69Abstract
Coronavirus (CoVs) is a type of enveloped RNA virus that is found in animals and humans. There are near about six different species of CoVs are available and all of them can cause different health issue to human. In human this virus can effect respiratory, hepatic, enteric and neurological system. The past Middle East respiratory syndrome coronavirus and severe acute respiratory syndrome coronavirus has been transmitted from animal to human. Presently there is a new strain of corona virus, named SARS-CoV-2, causing serious health crises to human. This virus is highly contagious and has resulted in a rapid pandemic of COVID-19. The number of infected people and death caused by COVID-19 is increasing day by day. This review will provide a detailed overview of COVID-19 and its serious effect to the human health.Keywords
Coronavirus, Virus, Health, SARS-CoV-2References
- K. Nalini Devi, Juliana Shanthi Rosy. ECMO therapy for COVID-19. Asian J. Nursing Education and Research. 2021; 11(2):299-301. Peiris JS, Lai ST, Poon LL, Guan Y, Yam LY, Lim W, et al. Lancet, 2003;361:1319–25.
- Subhashis Debnath, Runa Chakravorty, Donita Devi. COVID 19 and its management. Asian Journal of Pharmaceutical Research. 2021; 11(2):117-1.
- Archana B. Chavhan, Pavan S. Jadhav, Satish Shelke. COVID 19: Outbreak, Structure and Current therapeutic strategies. Asian J. Pharm. Tech. 2021; 11(1):76-83.
- Gurvishal Sinha. The vista of Pandemic in the world and its adaptation by Society: Statistical significant precautions on COVID. Asian Journal of Management. 2020;11(4):453-456.
- Ritik S. Jain, Tejas G. Jain, Suraj K. Ishikar. Impact of Covid-19 on Changing Habits and Health Issues of the Public. Asian Journal of Management. 2020;11(4):524-528.
- Niloy Sarkar, Bijoy Kumar Mandal, Soumya Paul. Activity, Effect on Human and Salvation from effect of COVID-19. Asian Journal of Management. 2021; 12(2):228-4.
- B. V. Naresh. A Review of the 2019 Novel Coronavirus (COVID-19) Pandemic. Asian J. Pharm. Res. 2020; 10(3):233-238.
- Vaishnavi. K. Patil, Azam. Z. Shaikh. Corona (Covid - 19). Asian J. Pharm. Res. 2020; 10(4):275-285.
- Vishwanath Biradar, Prerana Dalvi. Impact of COVID19 on Child Health: Parents Perspective. Int. J. Nur. Edu. and Research. 2020; 8(4):463-467.
- Atul Sharma, Keerthi Mohanan. Obstacles Faced by Nurses working in Covid-19 Unit: A Developing Country view Point. Asian J. Nursing Education and Research. 2020; 10(4):459-462.
- Darshana Kumari Wankhede. COVID-19- Problem faced by Indians during Lockdown. Asian J. Nursing Education and Research. 2020; 10(4):501-504.
- Melisa Fernandes, Jyoti R. Thakur, Manisha S. Gavanje. A Study to assess knowledge regarding covid-19 among Nursing students. Asian J. Nursing Education and Research. 2021; 11(1):65-67.
- Subhashis Debnath, Runa Chakravorty, Donita Devi. A Review on Role of Medicinal plants in Immune system. Asian J. Pharm. Tech. 2020; 10(4):273-277.
- Mayur S. Jain, Shashikant D. Barhate. Corona viruses are a family of viruses that range from the common cold to MERS corona virus: A Review. Asian J. Res. Pharm. Sci. 2020; 10(3):204-210.