Stomach Mimicry of A-Forte for Pharmacokinetic Insight
Keywords:
Drug absorption from solid dosage forms after oral administration depends on the release of the drug substance from the drug product, the dissolution or solubilization of the drug under physiological conditions, and the permeability across the gastrointesAbstract
Drug absorption from solid dosage forms after oral administration depends on the release of the drug substance from the drug product, the dissolution or solubilization of the drug under physiological conditions, and the permeability across the gastrointestinal tract. In vitro dissolution may be relevant to the prediction of in vivo performance. To evaluate the in vitro dissolution of A-forte, a siddha proprietary medicine and the influencing factors, a study of stomach mimicry for A-forte was undertaken. In the present study, the release of A-forte in different pH conditions by slow release and faster release pattern was studied. The release of actives was measured spectrophotometry. The possible variations caused because of A-forte to gastric media and influence of gastric media on A-forte was studied. Further the characteristics of various constituents of A-forte capsule released under different conditions were studied by Thin Layer Chromatography (TLC). The rate of dissolution of A-forte capsules was high in the low pH of 2 compared to high pH (4, 6.8). However, the pH of medium was decreased by excipient Phyllanthus emblica. pH altering property of Phyllanthus emblica may create an acidic micro-environment which may possibly cause gastric irritation. The herbal actives are however, not influenced by the pH and the rate of dissolution is unaffected by pH variation of medium as revealed by our subsequent TLC studies. The findings of the study are presented in the research paper.References
Sandra Alves de Sousa, Henrique Pascoa, Edemilson Cardoso da Conceição, et al. Dissolution Test of Herbal Medicines Containing Paullinia cupana: Validation of Methods for Quantification and Assessment of Dissolution. Braz J Pharm Sci. apr/jun, 2011; 47(2).
Fip Guidelines for Dissolution Testing of Solid Oral Products. Joint Report of the Section for Official Laboratories and Medicines Control Services and the Section of Industrial Pharmacists of the F.I.P. 1996; Drug Infom J. 30: 1071–1084p.
Gowthamarajan K, Sachin Kumar Singh, Dissolution Testing for Poorly Soluble Drugs: A Continuing Perspective. Dissolution Technologies | August 2010.
The European Agency for the Evaluation of Medicinal Products, Points to Consider on the Biopharmaceutical Characterization of Herbal Medicinal Products, 2003.
World Health Organization, Quality Control Methods for Medicinal Plant Materials, Geneva, 1998.
Guidelines for Adverse Drug Reaction (ADR) Reporting. Drug Administration and Control Authority (DACA), Addis Ababa, Ethiopia.
Rahul Kasar, Ashish Gogia, et al. Critical Factor That Governs a Successful TLC/HPTLC Analysis of Herbal Medicinal Products (HMPS). Research and Reviews: J Pharm Anal. October-December, 2013, 2(4).
Jacinda James, Ian Dubery. Identification and Quantification of Triterpenoid Centelloids in Centella asiatica (L.) Urban by Densitometric TLC. J Plan Chromatogr. 2011; 24: 82–87, 0933–4173p.
Parwez Alam, Jyoti Gupta, et al. A HPTLC Method for Qualitative and Quantitative Estimation of Gallic Acid from Emblica officinalis Gaertn in Polyherbal Formulation. Res J Pharm Biol Chem Sci. RJPBCS October – December 2012; 3(4): 1218p.
Mercè Bonfill, Susana Mangas, et al. Identification of Triterpenoid Compounds of Centella asiatica by Thin-layer Chromatography and Mass Spectrometry. Biomed. Chromatogr. Published online in Wiley Inter Science www.interscience.wiley.com).
DOI: 10.1002/bmc.564.
Shatwani Khyati, et al. A Preliminary Phyto-chemical Assay of Aswagandha Gransules: A Pilot Study. Int J Res Ayurveda Pharm. 2011; 2(4): 1026–1032p.
Kimberly Boyd Stallings BS. Mercury Release from Cinnabar in Water and Aqueous Solutions of Hydroquinone or Ascorbic Acid. [Thesis] Roosevelt University, 2009 M.S., University of Illinois at Chicago, Chicago, 2013.
Manayath Damodaran, Kesavapillai Ramakrishnan Nair. CXLVI. A Tannin from the Indian Gooseberry (Phyllanthus emblica) with a Protective Action on Ascorbic Acid. From the Biochemical Laboratory, University of Madras, Madras. (Received April 20th, 1936.), 1014–1020p.
The United States Pharmacopoeia/The National Formulary (USP 32/NF 27), Rockville, United States Pharmacopeial Convention, 2010.
Vivek kr ghosh, Shrinivas g bhope, et al. Development and Validation of Dissolution Test Method for Andrographolide from Film Coated Polyherbal Tablet Formulation. Int J Pharm Pharm Sci. 2012; 4(3): 307–312p. ISSN- 0975-1491. Received: 11 Jan 2012, Revised and Accepted: 11 Feb 2012.
Mehdi Ansari, Maryam Kazemipour, Javad Talebnia. The Development and Validation of a Dissolution Method for Clomipramine Solid Dosage Forms, Dissolution Technologies, August 2004
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