Literature DB >> 12661064

Timed-release formulation to avoid drug-drug interaction between diltiazem and midazolam.

Toyohiro Sawada1, Kazuhiro Sako, Keiichi Yoshihara, Katsutoshi Nakamura, Shigeharu Yokohama, Masahiro Hayashi.   

Abstract

The purpose of this study was to investigate whether the use of a timed-release (TR) drug formulation can avoid unfavorable pharmacokinetic drug-drug interactions in vivo. First, the effects of the time interval between administration of midazolam and diltiazem on the known drug-drug interaction between these drugs were investigated in dogs. When dogs were given midazolam orally at the same time they were orally given an aqueous diltiazem solution, the area under the plasma concentration-time curves of midazolam increased significantly compared with that of midazolam given orally in the absence of diltiazem. However, there was no significant difference in pharmacokinetics of midazolam when the diltiazem solution was administered 1-2 h after midazolam. Tests on a TR formulation containing diltiazem demonstrated that the first appearance of diltiazem in plasma occurs at 2.6 +/- 0.5 h in dogs. Subsequent tests showed that the plasma concentration-time profile of midazolam after concurrent oral administration of the diltiazem TR formulation was almost the same as that of midazolam administered alone. These results demonstrate that a TR formulation of diltiazem can avoid the interaction between diltiazem and midazolam by creating a time interval between absorption of drugs in vivo, without the need for closely controlling the time of drug administration. Copyright 2003 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 92:790-797, 2003

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12661064     DOI: 10.1002/jps.10336

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  5 in total

1.  Hollow microspheres for gastroretentive floating- pulsatile drug delivery: preparation and in vitro evaluation.

Authors:  Maryam Maghsoodi; Elham Hemati; Bahram Qadermazi; Zahra Yari
Journal:  Adv Pharm Bull       Date:  2011-12-15

2.  The influence of the copolymer composition on the diltiazem hydrochloride release from a series of pH-sensitive poly[(N-isopropylacrylamide)-co-(methacrylic acid)] hydrogels.

Authors:  Eva Díez-Peña; Paloma Frutos; Gloria Frutos; Isabel Quijada-Garrido; José Manuel Barrales-Rienda
Journal:  AAPS PharmSciTech       Date:  2004-04-20       Impact factor: 3.246

3.  Pharmacokinetics of the CYP 3A substrate simvastatin following administration of delayed versus immediate release oral dosage forms.

Authors:  Marija Tubic-Grozdanis; John M Hilfinger; Gordon L Amidon; Jae Seung Kim; Paul Kijek; Petra Staubach; Peter Langguth
Journal:  Pharm Res       Date:  2008-01-24       Impact factor: 4.200

4.  Supersaturated self-nanoemulsifying drug delivery systems (Super-SNEDDS) enhance the bioavailability of the poorly water-soluble drug simvastatin in dogs.

Authors:  Nicky Thomas; René Holm; Mats Garmer; Jens Jakob Karlsson; Anette Müllertz; Thomas Rades
Journal:  AAPS J       Date:  2012-11-21       Impact factor: 4.009

5.  Fixed Dose Single Tablet Formulation with Differential Release of Amlodipine Besylate and Simvastatin and Its Pharmacokinetic Profile: QbD and Risk Assessment Approach.

Authors:  Ummarah Kanwal; Shahid Mukhtar; Muzzamil Waheed; Arifa Mehreen; Nasir Abbas; Rahat Shamim; Khalid Hussain; Fatima Rasool; Amjad Hussain; Nadeem Irfan Bukhari
Journal:  Drug Des Devel Ther       Date:  2021-05-24       Impact factor: 4.162

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.