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- R. Meshram
- G. M. Khakse
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- N. L. Selokar
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- H. Agrawal
- A. K. Raja
- A. A. Sahare
- P. Palta
- M. S. Chauhan
- R. S. Manik
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Journals
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Priya, D.
- Nutritional Status and Blood Pressure among Adolescents in Miraj, Maharashtra
Abstract Views :301 |
PDF Views:268
Authors
Affiliations
1 Department of Community Medicine, S.V.N. Govt. Medical College, Yavatmal, IN
1 Department of Community Medicine, S.V.N. Govt. Medical College, Yavatmal, IN
Source
Indian Journal of Medicine and Healthcare, Vol 1, No 7 (2012), Pagination: 172-175Abstract
Objectives: Hypertension is the leading risk factor, ranking third for mortality rate. This study is to access the relationship between the childhood obesity which leads to hypertension during adolescents. Study design: A cross-sectional study was conducted at Miraj from August 2009 - September 2010, among 2370 adolescents in the age group of 10-19 yrs. A pre-designed, pre-tested structural questionnaire was used for data collection. Physical examination, which includes anthropometric measurements such as height, weight and blood pressure. Mean, standard deviation and χ2 test were used for statistical analysis. Results: The prevalence of hypertension was 1.1% and highest prevalence (2.9%) was observed in the age group of 18-19 years. Overall prevalence of obesity was 3.0%. The prevalence of hypertension was 26.7% in obese adolescents.Keywords
Nutritional Status, Blood Pressure, Hypertension, ObesityFull Text
References
- Munter P, He J, Cutler JA, Wildman RP and Whelton BK (2004) Trends in blood pressure among children and adolescents. JAMA. 291, 2107-2113.
- World health Organization (WHO) (1992). Hypertension control: report of a WHO Expert Committee. World Health Organization, Geneva 1992. WHO Technical Report Series No. 862, 1-83.
- World health Organization (WHO) (1985) Report of a WHO Study Group. Blood pressure studies in children. World Health Organization. Geneva 1985. Technical Report Series No 715.
- The World Health Report (2002) Reducing risks, promoting health life. Geneva, Switzerland. World Health Organization: Available from URL: http://www.who.int/whr/2002/en
- WHO, UNFPA, UNICEF (2010) Action for adolescent health: Towards a common agenda: Recommendations for a joint study group.
- Mano S Selvan and Anura V Kurpad (2004) Primary prevention: Why focus on children & young adolescents?. Indian J. Med. Res.120, 511-518.
- Kochanek KD and Smith BL (2004) Deaths. Preliminary data for 2002. Natl. Vital Stat Rep. 52, 1-47.
- Rames LK, Clarke WR, Connor WE, Reiter MA and Lauer RM (1978) Normal blood pressure and the evaluation of sustained blood pressure elevation in childhood: the muscatine study. Pediatrics. 61(2):245-51.
- Verma M, Chhatwal J and George S (1994) Obesity and hypertension in children. Indian Paed. 31, 1065-1069.
- Anand NK and Tandon L (1996) Prevalence of hypertension in school going children. Indian Paed. 33, 377-381.
- Qing He, Ding ZY, Fong DY and Karlberg J (2000) Blood pressure is associated with body mass index in both normal and obese children. Hypertension. 36, 165.
- Rosner B, Prineas R, Daniels SR and Loggie J (2000) Blood pressure differences between blacks and whites in relation to body size among US children and adolescents. Am. J. Epidemiol. 151(10),1007-1019.
- Sorof J and Daniels S (2002) Obesity hypertension in children: A problem of epidemic proportions. Hypertension. 40, 441-447.
- Mohan B, Kumar N, Aslam N, Rangbulla A, Kumbkarni S and Sood NK (2004) Prevalence of sustained hypertension and obesity in urban and rural school going children in Ludhiana. Indian Heart J. 56, 310-314.
- Kaur S, Kapil U and Singh P (2005) Pattern of chronic diseases amongst adolescent obese children in developing countries. Curr. Sci. 88(7), 1052-1056.
- Estimation of Yarn Hairiness using Image Processing
Abstract Views :169 |
PDF Views:4
Authors
Affiliations
1 Department of Placement at Sasurie College of Engineering, Tirupur, IN
2 Department of Computer Science Engineering, Easwari Engineering College, Anna University, Chennai, IN
1 Department of Placement at Sasurie College of Engineering, Tirupur, IN
2 Department of Computer Science Engineering, Easwari Engineering College, Anna University, Chennai, IN
Source
Digital Image Processing, Vol 6, No 8 (2014), Pagination: 337-341Abstract
Yarn hairiness is one of the significant quality parameter for producing quality fabrics .Fibers protruding out from the main body of the yarn is called hairiness. The upshot of yarn hairiness on the textile operations such as spinning, knitting, etc, led to the measurement of hairiness. This paper includes the analysis of cotton yarn [17], Lenin yarn and bamboo yarn. The hairiness analysis without charging leads to the problems of less accuracy in the hair count and the area of measurement. In the proposed system the videos of charged yarn is taken as input and frames are extracted. The yarn core extraction is performed using graph cut segmentation. Then by masking, the yarn hairs are extracted. The labeling of the yarn hair is done for the analysis of hair nature and for the parameter measurements like hair count, types of hairs and the length of hair. Through this analysis the yarn quality is estimated .Finally the other types of yarns can also be analyzed.
Keywords
Yarn Hairiness, Graph Cut, Linen Yarn.
- Milk-Derived Epithelial Cells Area a Potential Source of Donor Genome for the Production of Buffalo (Bubalus bubalis) Cloned Embryos
Abstract Views :299 |
PDF Views:77
Authors
N. L. Selokar
1,
M. Saini
1,
H. Agrawal
1,
A. K. Raja
1,
A. A. Sahare
1,
D. Priya
1,
P. Palta
1,
M. S. Chauhan
1,
R. S. Manik
1,
S. K. Singla
1
Affiliations
1 Animal Biotechnology Centre, National Dairy Research Institute, Karnal 132 001, IN
1 Animal Biotechnology Centre, National Dairy Research Institute, Karnal 132 001, IN
Source
Current Science, Vol 110, No 8 (2016), Pagination: 1411-1413Abstract
In most somatic cell nuclear transfer (SCNT) experiments, traditional skinderived fibroblast cells are commonly used as the donor genome. In addition, alternative sources of donor genome include those derived from hair follicles, colostrum/milk, blood and semen. Milk is easily obtained from live animals with out any biopsies and can be a safe mode of somatic cell source for those animals with high risk of bacterial infection. Therefore, milk-derived somatic cells may be an important source donor genome for the production of cloned embryos and for endangered species conservation programmes as part of genome resource banking. Recently, Golla et al.Full Text
- Efficient Energy and Power Consumption of 3-D Chip Multiprocessor with NUCA Architecture
Abstract Views :140 |
PDF Views:0
Authors
Affiliations
1 Department of ECE, Vel Tech Multitech, Avadi, Chennai – 54, Tamil Nadu, IN
1 Department of ECE, Vel Tech Multitech, Avadi, Chennai – 54, Tamil Nadu, IN
Source
Indian Journal of Science and Technology, Vol 9, No 2 (2016), Pagination:Abstract
Objective: Technology trend are one of the most important to use the bulky on-chip memories such as level-2 (L2) and level-3 (L3) cache. In this paper, Non-Uniform Cache access Architectures (NUCA) has been used in order to decrease the effects of the high access latencies. For the systems which operate at high frequency, the latencies of such caches are conquered by wire delays. Methods: In this architecture, several banks are partitioned and which is connected to the controller through switches and links. This larger cache memory increases overall wire delays across the chip due to very bulky latencies. The majority of the access time will not absorb them self and that occupy in the routing to and from the several banks. The predictable lower-level caches have the best ever access time among the entire the sub arrays, although such uniform cache access don’t make the use of differences in latencies of the entire sub arrays. Findings: Hence there is a necessitate for non-uniform cache architectures where the cache memories is broken down into several banks that can be analyzed at dissimilar latencies and resulting in diminish of energy and power consumption. Applications/Improvements: An experimental result shows the comparison of NUCA and UCA using SRAM/MRAM in terms of power and energy.
Keywords
Chip Multiprocessors, Non Uniform Cache Access, Uniform AccessFull Text
- OTP Generation for ATM Theft Protection
Abstract Views :123 |
PDF Views:6
Authors
Source
International Journal of Innovative Research and Development, Vol 3, No 6 (2014), Pagination:Abstract
Anself-governing ATM host has a right to use any bank. There is no security layer is implemented in the ATM card except pin number. It is very costly for the bank to include the fingerprint and Iris scanner. In this paper, we monitor the location of the ATM usage, time taken for the user to accessing the ATM machine, sequence of events processed by the user and expected amount of withdrawal by the user. All these four factors are verified for the authentication purpose of the user along with password. If any of the above said, parameter are differing and then the One Time Password is generated to the User’s Mobile number for further more secure authentication system. In the modification phase, an automation user Internet recognition model is designed to enhance the user comfort and detection of the time span spend by the user in the ATM machine. If due to signal problem of the mobile One Time Password will not be received in that cause secret process is used to private ATM users.
Keywords
ATM, Transaction, Identity theft, One Time Password, Secret processFull Text
- Green Chemistry Approach for the Synthesis of Some Benzimidazole Derivatives and their Biological Evaluation
Abstract Views :166 |
PDF Views:0
Authors
Affiliations
1 Department of Pharmaceutical Chemistry, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai, IN
1 Department of Pharmaceutical Chemistry, SRM College of Pharmacy, SRM Institute of Science and Technology, Kattankulathur, Chennai, IN
Source
Research Journal of Pharmacy and Technology, Vol 12, No 3 (2019), Pagination: 1023-1030Abstract
Microwave induced organic reactions are simple, fast, efficient and an economical method for the synthesis of organic molecules and has developed as a tool towards green chemistry. Microwave assistance can reduce the time of chemical reaction from hours to seconds. Benzimidazole nucleus owing to its wide range of biological activities anticipated to be an important pharmacophore in the modern drug discovery. Benzimidazole nucleus showing biological activities such as anti-convulsant, anti-inflammatory, anti-cancer etc., has made it an imperative anchor for development of modern therapeutic agents. Therefore six derivatives belonging to substituted benzimidazole were synthesized in one step microwave assistance and their structural integrity was confirmed by spectroscopy. The derivatives were evaluated in-vitro for free radical scavenging property, anti-microbial, cytotoxic activities. The free radical scavenging ability of synthesized compounds and standard ascorbic acid were tested using DPPH assay. The synthesized compounds 5(c), 5(d) and 5(f) possessed significant anti-oxidant property. The anti-microbial activity was assessed using two strains of gram positive and gram negative with standard tetracycline and the cytotoxic effect was performed using Brine shrimp lethality assay. Compounds 5(c), 5(d) and 5(f) showed significant anti-microbial action against gram positive and gram negative strains. LD50 was determined by cytotoxic assay using brine shrimp. Compounds 5(d) and 5(f) showed significant activity when compared with that of standard capacetabine. The results bespeak a new potential for benzimidazole derivatives as lead compounds to advance as medicinal agents.Keywords
Chemistry, Benzimidazoles, Anti-Oxidant, Anti-Microbial, Brine Shrimp Lethality Assay.References
- Kiumars Bahrami, Mehdi Khodaei M, Fardin Naali. Mild and Highly efficient method for the synthesis of 2-Arylbenzimidazoles and 2-Arylbenzothiazoles. Journal of organic chemistry. 2008; (73):6835–6837.
- Pranjal Gogoi, Dilip Konwar. An efficient and one pot synthesis of imidazolines and benzimidazoles via anaerobic oxidation of carbon-nitrogen binds in water. Tetrahedron letters. 2006; (47):79–82.
- Jie-Ping Wan,et al. Water mediated chemoselective synthesis of 1, 2-disubstituted benzimidazoles using o-phenylenediamine and the extended synthesis of quinoxalines. Journal of Green Chemistry. 2009; (11): 1633–1637.
- Kumaraswamy Gullapelli, et al. Synthesis of 1,3,5 triazinane-2-ones and 1,3,5 Oxadiazinane-2-ones linked with benzimidazoles. Asian Journal of Research in Chemistry 2017; 10(4), 0974-4169.
- Arun B. Chavan, et al. Solvent free U.V-Catalyzed Synthesis of Benzimimdazoles. Asian Journal of Research in Chemistry 2016; 9(10), 0974-4169.
- Atul R. Bendale,etal. Sonochemical Synthesis of 2, 3-Diphenylquinoxaline Using Different Catalysts, a Green Chemistry Approach. Asian Journal of Research in Chemistry. 2011; 4(6), 0974-4169.
- C. Thangavelu, et al. Sustainability of Potable Water System: Toward Green Chemistry and Green Technologies. Asian Journal of Research in Chemistry. 2011; 4(7), 0974-4169.
- Priyanka M. Patel, et al. Green Chemistry -An Overview. Asian Journal of Research in Chemistry 2013; 6(7), 0974-4169.
- Pankaj Kumar, et al. Synthesis and Antimicrobial evaluation of Some novel Mercapto Pyrimidine via Pyrrole chalcone. Research Journal of Pharmacy and Technology. 2018; 11(7): 0974-3618.
- Yogita Bansal, Om Silakari. The therapeutic journey of benzimidazoles. Bioorganic & Medicinal Chemistry. 2012; (20): 6208–6236.
- Rohit Tripathi, et al. Pharmacological activities of Benzimidazole derivatives - An Overview. Asian Journal of Research in Chemistry. 2013; 6(5), 0974-4169.
- Harti Jaouad, et al. Benzimidaoles and Pharmacological Activities: A Review. Research Journal of Pharmacy and Technology 2014; 7(4), 0974-3618.
- Priya D, Srimathi R. Synthesis and Characterization of Antimicrobial Activity of Novel Thiazolidinone Derivatives of 1, 2-Benzisoxazole. International Journal of Chem Tech Research. 2016; 9(9): 652-659.
- Salahuddin, Mohammad Shaharyar, Avijit Mazumder. Benzimidazoles: A biologically active compounds. Arabian Journal of Chemistry. 2017; (10): 157–173.
- CananKus, et al. Synthesis and antioxidant properties of novel N-methyl-1, 3, 4- thiadiazol-2-amine and 4-methyl-2H-1, 2, 4-triazole-3(4H)-thione derivatives of benzimidazole class. Bioorganic & Medicinal Chemistry. 2008; (16): 4294–4303.
- Muhammad Taha, et al. Synthesis, antiglycation and Antioxidant potentials of Benzimidazole Derivatives. Journal of King Saud University-Science. 2018; (18):1018-3647.
- Neda O. Anastassova, et al. Design, synthesis, antioxidant properties and mechanism of action of new N, N′- disubstituted benzimidazole-2-thione hydrazone derivatives. Journal of Molecular Structure. 2018; (18): 30416-2.
- Priya D, Srimathi R, Anjana G.V. Synthesis and evaluation of some mannich bases of Quinazolinone nucleus. Asian Journal of Pharmaceutical and Clinical Research. 2018; 11(2):407-409.
- Radha Krishan Arora, et al. Novel coumarin-benzimidazole derivatives as anti-oxidants and safer anti-inflammatory agents. Acta Pharmaceutica Sinica B. 2014; 4(5): 368-375.
- Anelia Ts. Mavrova, et al. Synthesis, electronic properties, antioxidant and antibacterial activity of some new benzimidazoles. Bioorganic & Medicinal Chemistry. 2015; (15): 30010-9.
- Xia-Bing Fu, et al. Cu (II)–dipeptide complexes of 2-(4′-thiazolyl) benzimidazole: Synthesis, DNA oxidative damage, antioxidant and in vitro antitumor activity. Journal of Inorganic Biochemistry. 2015; (143): 77–87.
- Lincy Joseph; Mathew George. Analgesic and Anti-Oxidant Activities of Certain (E)-3 Arylidene Flavanones Synthesized by One Pot Method. Asian Journal of Research in Chemistry 2009; 2(3), 0974-4169.
- Prashant N. Ubale; Sambhaji P. Vartale; Sandip G. Sontakke. Synthesis and anti-oxidant activity of some new substituted pyrazolo [ 4,5-e]-4H pyrimido[2,3-b] benzimidazoles. Asian Journal of Research in Chemistry 2016; 9(10), 0974-4169.
- Ya-Nan Wang, et al. Novel purine benzimidazoles as anti-microbial agents by regulating ROS generation and targeting clinically resistant Staphalococcus aureus DNA groove. Bioorganic and Medicinal Chemistry letters. 2018; (28):1621-1628.
- Snehlata Yadav, et al. Synthesis and evaluation of antimicrobial, antitubercular and anticancer activities of benzimidazole derivatives. Egyptian Journal of Basic and Applied Sciences. 2017.
- El-Gohary N S, Shaaban M I. Synthesis, antimicrobial, antiquorum-sensing and antitumor activities of new benzimidazole analogs. European Journal of Medicinal Chemistry. 2017; (17): 30435.
- Desai N C, et al. Synthesis, antibacterial and antitubercular activities of benzimidazole bearing substituted 2-pyridone motifs. European Journal of Medicinal Chemistry. 2014; (14): 00522-4.
- Xue-Jie Fang, et al. Synthesis and biological evaluation of 5-fluorouracil-derived benzimidazoles as novel type of potential antimicrobial agents. Bioorganic & Medicinal Chemistry Letters. 2016; (16): 30410-3.
- Sujit Kumar Mohantya, et al. Design, synthesis of novel azo derivatives of benzimidazole as potent antibacterial and anti tubercular agents. Beni-Suef University Journal of Basic and Applied Sciences. 2018;2314-8535.
- Niggula Praveen Kumar, et al. Synthesis of substituted phenanthrene-9-benzimidazole conjugates: Cytotoxicity evaluation and apoptosis inducing studies. European Journal of Medicinal Chemistry. 2017; (17): 30688-8.
- Rajan Abraham, et al. A novel series of N-acyl substituted indole-linked benzimidazoles and naphthoimidazoles as potential anti inflammatory, anti biofilm and anti microbial agents. Microbial Pathogenesis. 2017; 17: 31667-4.
- Mohan Rao Gangula and Vijaya Kumar Baru. Synthesis and Antimicrobial Activity of Some Novel N Mannich Bases of Substituted 2-Mercapto-1H-Benzimidazoles. 2012; 5(10), 0974-4150.
- Gopi C. and Dhanaraju M. D. Synthesis, Characterization and Anti-Microbial Evaluation of Derivative of Chalcone. Journal of Research in Chemistry 2011; 4(2), 0974-4169.
- Mohan Rao Gangula; Vijaya Kumar Baru. Synthesis and Antimicrobial Activity of Some Novel N-Mannich Bases of Substituted 2-Mercapto-1H-Benzimidazoles. Asian Journal of Research in Chemistry 2012; 5(10), 0974-4169.
- Santosh Dighe,et al. Synthesis and Evaluation of Some New Benzimidazole Derivatives for their Anti-Microbial and Anti-Inflammatory Activities. Asian Journal of Research in Chemistry 2014; 7(12), 0974-4169.
- Pratik P. Maske, et al. Synthesis and evaluation of 5,6-dinitro and 2-dialkylaminosubstituted benzimidazoles derivatives as potential antimicrobial agents. Asian Journal of Research in Chemistry 2015; 8(3), 0974-4169.
- K. Girija; B. Jamuna. Design and Synthesis of Some Novel Schiff’s Base Aryl Imidazole Derivatives, Characterization, Docking and Study of their Anti-Microbial Activity. Research Journal of Pharmacy and Technology 2015; 8(4), 0974-3618.
- Elif Apohan, et al. Synthesis, cytotoxic and antimicrobial activities of novel cobalt and zinc complexes of .benzimidazole derivatives. Journal of Organometallic Chemistry. 2016; (16): 30524-1.
- Seenaiah D, et al. Synthesis, antimicrobial and cytotoxic activities of pyrimidinyl benzoxazole, benzothiazole and benzimidazole. European Journal of Medicinal Chemistry 2014; (77): 1-7.
- Mirza Feroz Baig, et al. Iodine-catalyzed Csp3-H functionalization of methylhetarenes: One-pot synthesis and cytotoxic evaluation of heteroarenyl-benzimidazoles and benzothiazole. Bioorganic & Medicinal Chemistry Letters. 2017; (17): 30758-8.
- In silico Screening of Triphala Churna against Bacterial Agents
Abstract Views :156 |
PDF Views:74
Authors
Affiliations
1 Department of Pharmaceutical Chemistry, SRM College of Pharmacy, SRMIST, Kattankulathur, Kancheepuram – 603203, Tamil Nadu, IN
1 Department of Pharmaceutical Chemistry, SRM College of Pharmacy, SRMIST, Kattankulathur, Kancheepuram – 603203, Tamil Nadu, IN
Source
Journal of Natural Remedies, Vol 22, No 2 (2022), Pagination: 221 - 232Abstract
Triphala Churna consisting Triphala and its constituents have been revealed to have antibacterial properties against human pathogens. The phenolic ring of phytochemicals has been confirmed to be toxic against microorganisms and hence responsible for antibacterial effect. It has also been found to possess antimicrobial, anti-inflammatory, anti-oxidant, and other properties. The objective of this project is to investigate which bioactive compounds of Triphala churna have antibacterial action and can protect humans from infection. The majority of the molecules in phytochemical examination were positive for ethanolic and acetone extracts and the physicochemical characteristics were within the acceptable limits. In silico data clearly explains that the compounds of Triphala churna follows Lipinski’s rule of five. The toxicity profile and ADME parameters of the compounds revealed that most of the compounds were nontoxic towards carcinogenicity, mutagenicity, and reproductive effect. Based on the energy type of interaction between these molecules and the study protein, molecular docking revealed that the three compounds from Triphala churna own the highest docking score against InhA protein: Terflavin B (-9.67 Kcal/mol), Ellagic acid (-9.37 Kcal/mol), and Corilagin (-8.57 Kcal/mol).Keywords
Anti-bacterial Activity, InhA, Molecular Docking, Terflavin B, Triphala ChurnaFull Text
References
- Peterson CT, Denniston K, Chopra D. Therapeutic uses of Triphala in Ayurvedic medicine. J Altern Complement Med. 2017; 23(8):607–14. https://doi.org/10.1089/acm.2017.0083. PMid:28696777. PMCid:PMC5567597
- Nayak K, Patil A, Vishnuprasad S, Nayak DM. Antibacterial effect of triphala churna against common wound pathogens. Int J Curr Res. 2015; 7(01):12074–7.
- Singh RK, Gupta R, Dwivedi N. A review on antimicrobial activities of triphala and its constituents. World J Pharm Pharm Sci. 2016; 5(4):535–58.
- Rao PP. Antioxidant effect of Triphala - Critical review. J Ayurveda Integr Med. 2017; 2(1):213–19. https://doi.org/10.21760/jaims.v2i1.7513
- Prabu D, Kirubanandan S, Ponnudurai K, Nappinnai M, Jinu A, Renganathan S. Anti-inflammatory and analgesic activities of methanol extract of Triphala - A poly herbal formulation. Orient Pharm Exp Med. 2008; 8(4):423–9. https://doi.org/10.3742/OPEM.2008.8.4.423
- Chouhan B, Kumawat R, Kotecha M, Ramamurthy A, Nathani S. Triphala: A comprehensive ayurvedic review triphala: A comprehensive ayurvedic review. Int. J. Ayurveda Res. 2013; 4(4):612–17. https://doi.org/10.7897/2277-4343.04433
- Varma SR, Sivaprakasam TO, Mishra A, et al. Protective effects of Triphala on dermal fibroblasts and human keratinocytes. PLoS One. 2016; 11(1):e0145921. https://doi.org/10.1371/journal.pone.0145921. PMid:26731545 PMCid:PMC4711708
- Belapurkar P, Goyal P, Tiwari-Barua P. Immunomodulatory effects of triphala and its individual constituents: A review. Indian J Pharm Sci. 2014; 76(6):467–75.
- Prasad S, Srivastava S. Oxidative stress and cancer: Chemopreventive and therapeutic role of triphala. Antioxidants. 2020; 9(1):72. https://doi.org/10.3390/antiox9010072. PMid:31941067 PMCid:PMC7022920
- Murthy M. Anticancer and pro‐apoptotic effects of Triphala extract in human breast cancer MCF‐7 cells. FASEB J. 2018; 32(S1). https://doi.org/10.1096/fasebj.2018.32.1_supplement.151.2
- Chainani S, Siddana S, Reddy C, Thippeswamy M, Maurya M, Rudraswamy S. Antimicrobial activity of Triphala on Lactobacilli and Candida albicans: An in vitro study. J Orofac Sci. 2015; 7(2):104. https://doi.org/10.4103/0975-8844.169757
- Manoraj A, Thevanesam V, Bandara BMR, Ekanayake A, Liyanapathirana V. Synergistic activity between Triphala and selected antibiotics against drug resistant clinical isolates. BMC Complement Altern Med. 2019; 19(1):199. https://doi.org/10.1186/s12906-019-2618-1. PMid:31375093 PMCid:PMC6679468
- Rao P. Antioxidant effect of Triphala - Critical review. J Ayurveda Integr Med. 2017: 2(1). https://doi.org/10.21760/jaims.v2i1.7513
- Patil SG, Deshmukh AA, Padol AR, Kale DB. In vitro antimicrobial activity of Emblica officinalis fruit by tube dilution method. Toxicol Appl Pharmacol. 2012; 2:49–51
- Mahalakshmi K, Prabhakar J, Sukumaran VG. Antibacterial activity of Triphala, GTP and curcumin on Enterococci faecalis. Biomedicine. 2006; 26:43–6.
- Sumathi P, Parvathi A. Antibacterial potential of the three medicinal fruits used in Triphala: An Ayurvedic formulation. J. Med. Plants Res. 2010; 4:1682–5.
- Zareen N, Jaiganesh R. Antimicrobial effect of Triphala on oral microbes - An in vivo study. Drug Invent Today. 2019;11(2).
- Chainani S, Siddana S, Reddy C, Thippeswamy M, Maurya M, Rudraswamy S. Antimicrobial activity of Triphala on Lactobacilli and Candida albicans: An in vitro study. J Orofac Sci. 2015; 7(2):104. https://doi.org/10.4103/0975-8844.169757
- Kumar NS, Nair AS, Murali M, Devi PSS. Qualitative phytochemical analysis of triphala extracts. J. Pharmacogn Phytochem. 2017; 6(3):248–51.
- Duchowicz PR, Talevi A, Bellera C, Bruno-Blanch LE, Castro EA. Application of descriptors based on Lipinski’s rules in the QSPR study of aqueous solubilities. Bioorg Med Chem. 2007; 15(11):3711–9. https://doi.org/10.1016/j. bmc.2007.03.044. PMid:17418580
- Pires DEV, Blundell TL, Ascher DB. PkCSM: Predicting smallmolecule pharmacokinetic and toxicity properties using graph-based signatures. J Med Chem. 2015; 58(9):4066–72. https://doi.org/10.1021/acs.jmedchem.5b00104. PMid:25860834 PMCid:PMC4434528
- Kumar N, Mishra SS, Sharma CS, Singh HP, Singh H. In silico pharmacokinetic, bioactivity and toxicity evaluation of some selected anti-ulcer agents. Int J Pharm Sci Drug Res. 2017; 9(2). https://doi.org/10.25004/IJPSDR.2017.090205