FABRICATION AND ASSESSMENT OF LERCANIDIPINE HYDROCHLORIDE SOLID DISPERSIONS FOR SOLUBILITY PREFERMENT USING POLYMER COMBINATION
DOI:
https://doi.org/10.22159/ajpcr.2021.v14i7.41972Keywords:
Lercanidipine, Polymer, Solid dispersions, DissolutionAbstract
Objective: An attempt has made in fabricating solid dispersions (SDs) by taking lercanidipine hydrochloride (LCD) as a model drug.
Methods: The SDs were made using a poly mix of poly vinyl pyrrolidone (PVP) K-30, Poloxamer-188, and hydroxy propyl methyl cellulose (HPMC) K4M. Different proportions of LCD: polymer mix in 1:1, 1:3, 1:5, and 1:7 ratios were fabricated as SDs by solvent evaporation and melting method, further compressed into tablets. The LCD SDs were assessed for physicochemical, and LCD release possessions.
Results: The results were observed to be attractive with the increase in solubility LCD SD (F-3 and F-7) with 1:5 ratios of LCD.
Conclusion: The study concludes that the poly mix of PVP K-30, Poloxamer-188, and HPMC K4M and was found to be a better combination for elevating the solubility and release of LCD from the SDs.
Downloads
References
Lam JK, Xu Y, Worsley A, Wong IC. Oral transmucosal drug delivery for pediatric use. Adv Drug Deliv Rev 2014;73:50-62. DOI: https://doi.org/10.1016/j.addr.2013.08.011
Shah I, Bhatt S, Yadav A. Enhancement of solubility and dissolution of nebivolol by solid dispersion technique. Int J Pharm Pharm Sci 2014;6:566-71.
Hardikar SR, Mulla SS. Optimization of formulation of solid dispersion of furosemide by factorial design. Int J Pharm Pharm Sci 2020;12:43-8. DOI: https://doi.org/10.22159/ijpps.2020v12i4.36428
Ramasahayam B, Eedara BB, Kandadi P, Jukanti R, Bandari S. Development of isradipine loaded self-nano emulsifying powders for improved oral delivery: In vitro and in vivo evaluation. Drug Dev Ind Pharm 2015;41:753-63. DOI: https://doi.org/10.3109/03639045.2014.900081
Nabel EG. Cardiovascular disease. N Engl J Med 2003;349:60-72. DOI: https://doi.org/10.1056/NEJMra035098
Virdis A, Ghiadoni L, Taddei S. Effects of antihypertensive treatment on endothelial function. Curr Hyperten Rep 2011;13:276-81. DOI: https://doi.org/10.1007/s11906-011-0207-x
Annepogu H, Hindustan Abdul AH, Nayakanti D. Determining the best poloxamer carrier for thiocolchicoside solid dispersions. Turk J Pharm Sci 2020;17:372. DOI: https://doi.org/10.4274/tjps.galenos.2019.78800
Wu JX, Yang M, van den Berg F, Pajander J, Rades T, Rantanen J. Influence of solvent evaporation rate and formulation factors on solid dispersion physical stability. Eur J Pharm Sci 2011;44:610-20. DOI: https://doi.org/10.1016/j.ejps.2011.10.008
Mesnukul A, Yodkhum K, Mahadlek J, Phaechamud T. Characterization of indomethacin release from polyethylene glycol tablet fabricated with mold technique. Indian J Pharm Sci 2010;72:92. DOI: https://doi.org/10.4103/0250-474X.62255
Brooks RF, Dinsdale AT, Quested PN. The measurement of viscosity of alloys-a review of methods, data and models. Measur Sci Technol 2005;16:354. DOI: https://doi.org/10.1088/0957-0233/16/2/005
Patel J, Dhingani A, Garala K, Raval M, Sheth N. Quality by design approach for oral bioavailability enhancement of irbesartan by self-nanoemulsifying tablets. Drug Deliv 2014;21:412-35. DOI: https://doi.org/10.3109/10717544.2013.853709
Won DH, Kim MS, Lee S, Park JS, Hwang SJ. Improved physicochemical characteristics of felodipine solid dispersion particles by supercritical anti-solvent precipitation process. Int J Pharm 2005;301:199-208. DOI: https://doi.org/10.1016/j.ijpharm.2005.05.017
Ghareeb MM, Abdulrasool AA, Hussein AA, Noordin MI. Kneading technique for preparation of binary solid dispersion of meloxicam with poloxamer 188. AAPS PharmSciTech 2009;10:1206-15. DOI: https://doi.org/10.1208/s12249-009-9316-0
Kumar R, Patil MB, Patil SR, Paschapur MS, Mahalaxmi R. Development and characterization of orodispersible tablets of aceclofenac by sublimation technique. Int J PharmTech Res 2009;1:210-4.
Dong Z, Chatterji A, Sandhu H, Choi DS, Chokshi H, Shah N. Evaluation of solid state properties of solid dispersions prepared by hot-melt extrusion and solvent co-precipitation. Int J Pharm 2008;355: 141-9. DOI: https://doi.org/10.1016/j.ijpharm.2007.12.017
Charde S, Mudgal M, Kumar L, Saha R. Development and evaluation of buccoadhesive controlled release tablets of lercanidipine. AAPS PharmSciTech 2008;9:182-90. DOI: https://doi.org/10.1208/s12249-007-9031-7
Shaikh F, Patel V, Patel M, Surt N. Dissolution method development and validation for lercanidipine hydrochloride tablets. Dissolut Technol 2018;25:38-46. DOI: https://doi.org/10.14227/DT250118P38
Published
How to Cite
Issue
Section
Copyright (c) 2021 NAZEMOON REDDY
This work is licensed under a Creative Commons Attribution 4.0 International License.
The publication is licensed under CC By and is open access. Copyright is with author and allowed to retain publishing rights without restrictions.