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甲芬那酸固体分散体的体外溶出度研究

In vitro Dissolution Studies on Solid Dispersions of Mefenamic Acid.

作者信息

Rao K R S Sambasiva, Nagabhushanam M V, Chowdary K P R

机构信息

Achrya Nagarjuna University, Nagarjunanagar-522 510, Guntur, India.

出版信息

Indian J Pharm Sci. 2011 Mar;73(2):243-7. doi: 10.4103/0250-474x.91575.

DOI:10.4103/0250-474x.91575
PMID:22303074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3267315/
Abstract

Solid dispersions of mefanamic acid with a water-soluble polymer polyvinyl pyrrolidine and a super disintegrant, primojel were prepared by common solvent and solvent evaporation methods employing methanol as the solvent. The dissolution rate and dissolution efficiency of the prepared solid dispersions were evaluated in comparison to the corresponding pure drug. Solid dispersions of mefenamic acid showed a marked enhancement in dissolution rate and dissolution efficiency. At 1:4 ratio of mefenamic acid-primojel a 2.61 fold increase in the dissolution rate of mefenamic acid was observed with solid dispersion. The solid dispersions in combined carriers gave much higher rates of dissolution than super disintegrants alone. Mefanamic acid-primojel-polyvinyl pyrrolidine (1:3.2:0.8) solid dispersion gave a 4.11 fold increase in the dissolution rate of mefenamic acid. Super disintegrants alone or in combination with polyvinyl pyrrolidine could be used to enhance the dissolution rate of mefenamic acid.

摘要

以甲醇为溶剂,采用共溶剂法和溶剂蒸发法制备了甲芬那酸与水溶性聚合物聚乙烯吡咯烷酮以及超级崩解剂优特奇的固体分散体。与相应的纯药物相比,对所制备的固体分散体的溶出速率和溶出效率进行了评估。甲芬那酸固体分散体的溶出速率和溶出效率显著提高。在甲芬那酸与优特奇比例为1:4时,观察到固体分散体中甲芬那酸的溶出速率提高了2.61倍。复合载体中的固体分散体比单独使用超级崩解剂的溶出速率高得多。甲芬那酸-优特奇-聚乙烯吡咯烷酮(1:3.2:0.8)固体分散体使甲芬那酸的溶出速率提高了4.11倍。单独使用超级崩解剂或与聚乙烯吡咯烷酮联合使用均可提高甲芬那酸的溶出速率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f266/3267315/82f50d4d13a6/IJPhS-73-243-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f266/3267315/853e23d142ba/IJPhS-73-243-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f266/3267315/69d4efac8894/IJPhS-73-243-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f266/3267315/82f50d4d13a6/IJPhS-73-243-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f266/3267315/853e23d142ba/IJPhS-73-243-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f266/3267315/69d4efac8894/IJPhS-73-243-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f266/3267315/82f50d4d13a6/IJPhS-73-243-g009.jpg

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本文引用的文献

1
Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs.固体分散体作为提高难溶性药物口服生物利用度的策略。
Drug Discov Today. 2007 Dec;12(23-24):1068-75. doi: 10.1016/j.drudis.2007.09.005. Epub 2007 Oct 30.
2
Kinetic study of the transformation of mefenamic acid polymorphs in various solvents and under high humidity conditions.甲芬那酸多晶型物在各种溶剂及高湿度条件下转化的动力学研究。
Int J Pharm. 2006 Sep 14;321(1-2):18-26. doi: 10.1016/j.ijpharm.2006.04.020. Epub 2006 May 12.
3
Physicochemical and crystallographic characterization of mefenamic acid complexes with alkanolamines.
Influence of the microwave technology on solid dispersions of mefenamic acid and flufenamic acid.
微波技术对甲芬那酸和氟芬那酸固体分散体的影响。
PLoS One. 2017 Jul 31;12(7):e0182011. doi: 10.1371/journal.pone.0182011. eCollection 2017.
4
Improvement in Dissolution Rate of Cefuroxime Axetil by using Poloxamer 188 and Neusilin US2.使用泊洛沙姆188和纽西龙US2提高头孢呋辛酯的溶出速率
Indian J Pharm Sci. 2013 Jan;75(1):67-75. doi: 10.4103/0250-474X.113551.
5
Improved dissolution and anti-inflammatory effect of ibuprofen by solid dispersion.固体分散体提高布洛芬的溶出度和抗炎效果。
Front Med. 2012 Jun;6(2):195-203. doi: 10.1007/s11684-012-0189-3. Epub 2012 May 9.
J Pharm Sci. 2004 Jan;93(1):144-54. doi: 10.1002/jps.10468.
4
STUDIES ON ABSORPTION OF EUTECTIC MIXTURE. II. ABSORPTION OF FUSED CONGLOMERATES OF CHLORAMPHENICOL AND UREA IN RABBITS.共熔混合物的吸收研究。II. 家兔对氯霉素与尿素熔融聚集体的吸收
Chem Pharm Bull (Tokyo). 1964 Feb;12:134-44. doi: 10.1248/cpb.12.134.
5
Disease-drug interaction: Reduced response to propranolol despite increased concentration in the rat with inflammation.疾病-药物相互作用:尽管在炎症大鼠体内普萘洛尔浓度升高,但对其反应降低。
J Pharm Sci. 2003 May;92(5):1077-84. doi: 10.1002/jps.10381.
6
Effect of compaction pressure on the dissolution efficiency of some direct compression systems.压制压力对某些直接压片系统溶出效率的影响。
Pharm Acta Helv. 1972 Oct;47(10):594-607.