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2-羟丙基-β-环糊精可提高全反式维甲酸的水溶性和光稳定性。

2-hydroxypropyl-beta-cyclodextrin increases aqueous solubility and photostability of all-trans-retinoic acid.

作者信息

Lin H S, Chean C S, Ng Y Y, Chan S Y, Ho P C

机构信息

Department of Pharmacy, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260.

出版信息

J Clin Pharm Ther. 2000 Aug;25(4):265-9. doi: 10.1046/j.1365-2710.2000.00285.x.

Abstract

BACKGROUND

All-trans-retinoic acid (ATRA, vitamin A acid or tretinoin) is effective in the treatment of acute promyelocytic leukaemia (APL). Unfortunately, the oral absorption of ATRA is highly variable. Its poor aqueous solubility also makes it difficult to be formulated into parenteral formulation. To date, there is no parenteral formulation of ATRA available commercially.

OBJECTIVE

To undertake the preformulation work necessary for developing such a product.

METHOD

We investigated the solubility and stability profile of ATRA in various formulations.

RESULTS

The aqueous solubility of ATRA could be greatly increased by the inclusion of ATRA in 2-hydroxypropyl-beta-cyclodextrin (HP-beta-CD). Adjusting the pH value further improved the water solubility of ATRA. The photostability of HP-beta-CD-based formulation of ATRA was evaluated and it was found that inclusion ATRA into HP-beta-CD did improve the photostability of ATRA.

CONCLUSION

These results showed that it is possible to develop a parenteral formulation and/or an aqueous oral formulation of all-trans-retinoic acid by using 2-hydroxypropyl-beta-cyclodextrin. However, the biopharmaceutical properties of such a formulation would be necessary before its use.

摘要

背景

全反式维甲酸(ATRA,维生素A酸或维甲酸)在急性早幼粒细胞白血病(APL)的治疗中有效。不幸的是,ATRA的口服吸收差异很大。其较差的水溶性也使其难以制成肠胃外制剂。迄今为止,尚无市售的ATRA肠胃外制剂。

目的

开展开发此类产品所需的处方前研究工作。

方法

我们研究了ATRA在各种制剂中的溶解度和稳定性。

结果

将ATRA包合于2-羟丙基-β-环糊精(HP-β-CD)中可大大提高其水溶性。调节pH值可进一步改善ATRA的水溶性。对基于HP-β-CD的ATRA制剂的光稳定性进行了评估,发现将ATRA包合于HP-β-CD中确实提高了ATRA的光稳定性。

结论

这些结果表明,通过使用2-羟丙基-β-环糊精开发全反式维甲酸的肠胃外制剂和/或水性口服制剂是可能的。然而,在使用前需要了解此类制剂的生物药剂学性质。

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