Literature DB >> 9646283

Micronization: a method of improving the bioavailability of poorly soluble drugs.

J C Chaumeil1.   

Abstract

For poorly soluble drugs, the digestive absorption depends on their rate of dissolution. Decreasing the particle size of these drugs improves their rate of dissolution. Fine grinding mills are use to micronize powders: either jar mills or fluid energy mills. Theses processes were applied to griseofulvin, progesterone, spironolactone and diosmin. For each drug, micronization improved their digestive absorption, and consequently their bioavailability and clinical efficacy.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9646283

Source DB:  PubMed          Journal:  Methods Find Exp Clin Pharmacol        ISSN: 0379-0355


  21 in total

Review 1.  Impact of excipient interactions on drug bioavailability from solid dosage forms.

Authors:  Ravikiran Panakanti; Ajit S Narang
Journal:  Pharm Res       Date:  2012-05-19       Impact factor: 4.200

2.  NanoCrySP technology for generation of drug nanocrystals: translational aspects and business potential.

Authors:  Ganesh Shete; Arvind Kumar Bansal
Journal:  Drug Deliv Transl Res       Date:  2016-08       Impact factor: 4.617

Review 3.  Role of solvents in improvement of dissolution rate of drugs: crystal habit and crystal agglomeration.

Authors:  Maryam Maghsoodi
Journal:  Adv Pharm Bull       Date:  2015-03-05

4.  Gliclazide microcrystals prepared by two methods of in situ micronization: pharmacokinetic studies in diabetic and normal rats.

Authors:  Roya Talari; Jaleh Varshosaz; Saied Abolfazl Mostafavi; Ali Nokhodchi
Journal:  AAPS PharmSciTech       Date:  2010-05-05       Impact factor: 3.246

Review 5.  An overview on in situ micronization technique - An emerging novel concept in advanced drug delivery.

Authors:  K R Vandana; Y Prasanna Raju; V Harini Chowdary; M Sushma; N Vijay Kumar
Journal:  Saudi Pharm J       Date:  2013-05-29       Impact factor: 4.330

6.  Effect of cryogrinding on chemical stability of the sparingly water-soluble drug furosemide.

Authors:  Karolina Adrjanowicz; Kamil Kaminski; Katarzyna Grzybowska; Lukasz Hawelek; Marian Paluch; Irena Gruszka; Daniel Zakowiecki; Wieslaw Sawicki; Przemyslaw Lepek; Wojciech Kamysz; Lukasz Guzik
Journal:  Pharm Res       Date:  2011-06-25       Impact factor: 4.200

Review 7.  Process optimization and particle engineering of micronized drug powders via milling.

Authors:  A Brunaugh; H D C Smyth
Journal:  Drug Deliv Transl Res       Date:  2018-12       Impact factor: 4.617

Review 8.  Deciphering the divergent roles of progestogens in breast cancer.

Authors:  Jason S Carroll; Theresa E Hickey; Gerard A Tarulli; Michael Williams; Wayne D Tilley
Journal:  Nat Rev Cancer       Date:  2016-11-25       Impact factor: 60.716

9.  Effect of surface chemistry on nanoparticle interaction with gastrointestinal mucus and distribution in the gastrointestinal tract following oral and rectal administration in the mouse.

Authors:  Katharina Maisel; Laura Ensign; Mihika Reddy; Richard Cone; Justin Hanes
Journal:  J Control Release       Date:  2014-11-04       Impact factor: 9.776

10.  Using cocrystals to systematically modulate aqueous solubility and melting behavior of an anticancer drug.

Authors:  Christer B Aakeröy; Safiyyah Forbes; John Desper
Journal:  J Am Chem Soc       Date:  2009-12-02       Impact factor: 15.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.