Enhanced oral bioavailability of valsartan in rats using a supersaturable self-microemulsifying drug delivery system with P-glycoprotein inhibitors
Author:
Affiliation:
1. College of Pharmacy, Chung-Ang University, Seoul, Korea;
2. College of Pharmacy, Kyungsung University, Busan, Korea;
3. College of Pharmacy, Keimyung University, Daegu, Korea
Publisher
Informa UK Limited
Subject
Pharmaceutical Science,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/10837450.2019.1683749
Reference53 articles.
1. Oral absorption of a valsartan-loaded spray-dried emulsion based on hydroxypropylmethyl cellulose
2. QbD-Oriented Development of Self-Nanoemulsifying Drug Delivery Systems (SNEDDS) of Valsartan with Improved Biopharmaceutical Performance
3. Characterization of jejunal absorption and apical efflux of ropivacaine, lidocaine and bupivacaine in the rat using in situ and in vitro absorption models
4. Design and Evaluation of Self-Microemulsifying Drug Delivery System (SMEDDS) of Tacrolimus
5. Pharmacokinetic interaction study between quercetin and valsartan in rats andin vitromodels
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