Pharmacokinetic profile of BA-SD and BBA-SD.

NIAID Data Ecosystem2026-03-08 收录

药物制剂优化

口服生物利用度

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资源简介：

The pharmacokinetic parameters of BA free drug and BA-SD formulations groups after oral administration of 100 mg/kg.

创建时间：

2014-03-10

Design and optimization of novel in situ gel of mercaptopurine for sustained drug delivery

药物传递系统

药物制剂优化

Mercaptopurine is a purine antagonist, belonging to the class of antimetabolites. Its oral absorption is erratic and variable throughout GIT, with bioavailability of 5-37% and belongs to Biopharmaceut

DataCite Commons2021-03-27 更新70

Effects of granule particle size and lubricant concentration on tablet hardness containing large concentration of polymers

片剂配方工艺

药物制剂优化

ABSTRACT The objective of this research work is to demonstrate the impact of granule size and lubricant concentration on the hardness of tablets in formulations containing higher concentration of poly

NIAID Data Ecosystem20

Characteristic properties of optimized co-trimoxazole ODT.

药物制剂优化

口腔崩解片特性

Characteristic properties of optimized co-trimoxazole ODT.

Figshare2021-03-16 更新10

In vitro lipolysis/microsomal metabolism approach for the prediction of oral bioavailability of BCS II drugs in lipidic formulations

药物制剂优化

生物利用度预测

Lipidic formulations (LFs) are increasingly utilized for the delivery of drugs that belong to class II of the Biopharmaceutics Classification System (BCS). The current work proposes, for the first tim

DataCite Commons2024-11-29 更新60

A New Low Melting-Point Polymorph of Fenofibrate Prepared via Talc Induced Heterogeneous Nucleation

多晶型控制

药物制剂优化

Fenofibrate is one of the most commonly prescribed hyperlipidemia agents. Despite its high lipophilicity and ultralow aqueous solubility, most commercially available formulations use micronized crysta

Figshare2016-02-12 更新20

Pharmacokinetic profile of BA-SD and BBA-SD.

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