Literature DB >> 12751636

Dissolution behavior of a poorly water soluble compound in the presence of Tween 80.

Linna R Chen1, James A Wesley, Shobha Bhattachar, Bienvenido Ruiz, Korey Bahash, Suresh R Babu.   

Abstract

PURPOSE: To investigate the mechanism by which Tween 80 impedes the dissolution of CI-1041, a poorly water-soluble compound in its free form.
METHODS: Bulk powder and intrinsic dissolution (ID) of CI-1041 in 0.1 N HCl with various concentrations of Tween 80 were conducted. The residual solids of the dissolution experiments were characterized. The surface tension and the critical micellar concentration (CMC) of Tween 80 in 0.1 N HCl were determined.
RESULTS: CI-1041 underwent solvent mediated conversion to its chloride salt (CS) in 0.1 N HCl. The coating of the CS on the surface of the CI-1041 pellet decreased the ID rate 20 to 30 fold. When the Tween 80 concentration in 0.1 N HCl was below 0.5 mg/ml, the CS formation rate increased with increasing Tween 80 concentration. Above 0.5 mg/ml of Tween 80 in 0.1 N HCl, opposite trend was observed. The change in trend at 0.5 mg/ml Tween 80 coincided approximately with the CMC of Tween 80 in 0.1 N HCl.
CONCLUSIONS: The authors propose the following mechanism mediated by Tween 80. Below CMC, reduced surface tension caused by addition of Tween 80 increases the rate of nucleation of insoluble CS, causing the formation of CS on the surface of the CI-1041 free form. This, in turn, decreases the dissolution rate by decreasing the release of compound into solution. Above CMC, the effect of reduced surface tension on the CS nucleation and therefore its formation may be negated by other factors, such as an increase in viscosity or adsorption of surfactant on the crystal surface.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12751636     DOI: 10.1023/a:1023493821302

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  4 in total

Review 1.  Significance of controlling crystallization mechanisms and kinetics in pharmaceutical systems.

Authors:  N Rodríguez-Hornedo; D Murphy
Journal:  J Pharm Sci       Date:  1999-07       Impact factor: 3.534

2.  Physicochemical properties and bioavailability of carbamazepine polymorphs and dihydrate.

Authors:  Y Kobayashi; S Ito; S Itai; K Yamamoto
Journal:  Int J Pharm       Date:  2000-01-05       Impact factor: 5.875

3.  Physical characterization of nedocromil sodium hydrates.

Authors:  R Khankari; L Chen; D J Grant
Journal:  J Pharm Sci       Date:  1998-09       Impact factor: 3.534

4.  Dissolution of theophylline monohydrate and anhydrous theophylline in buffer solutions.

Authors:  J H de Smidt; J G Fokkens; H Grijseels; D J Crommelin
Journal:  J Pharm Sci       Date:  1986-05       Impact factor: 3.534

  4 in total
  12 in total

1.  Use of surfactants as plasticizers in preparing solid dispersions of poorly soluble API: stability testing of selected solid dispersions.

Authors:  Alazar N Ghebremeskel; Chandra Vemavarapu; Mayur Lodaya
Journal:  Pharm Res       Date:  2006-08       Impact factor: 4.200

2.  Mathematical Models to Explore Potential Effects of Supersaturation and Precipitation on Oral Bioavailability of Poorly Soluble Drugs.

Authors:  Mary S Kleppe; Kelly M Forney-Stevens; Roy J Haskell; Robin H Bogner
Journal:  AAPS J       Date:  2015-04-08       Impact factor: 4.009

3.  Solution-mediated phase transformation of haloperidol mesylate in the presence of sodium lauryl sulfate.

Authors:  Kristyn Greco; Robin Bogner
Journal:  AAPS PharmSciTech       Date:  2011-07-06       Impact factor: 3.246

4.  Implementing quality by design in pharmaceutical salt selection: a modeling approach to understanding disproportionation.

Authors:  Jeremy M Merritt; Shekhar K Viswanath; Gregory A Stephenson
Journal:  Pharm Res       Date:  2012-08-24       Impact factor: 4.200

5.  Design and Evaluation of Two-Step Biorelevant Dissolution Methods for Docetaxel Oral Formulations.

Authors:  Brijesh Shah; Xiaowei Dong
Journal:  AAPS PharmSciTech       Date:  2022-04-19       Impact factor: 4.026

6.  Implication of NMDA receptors in the antidyskinetic activity of cabergoline, CI-1041, and Ro 61-8048 in MPTP monkeys with levodopa-induced dyskinesias.

Authors:  Bazoumana Ouattara; Samah Belkhir; Marc Morissette; Mehdi Dridi; Pershia Samadi; Laurent Grégoire; Leonard T Meltzer; Thérèse Di Paolo
Journal:  J Mol Neurosci       Date:  2008-08-14       Impact factor: 3.444

7.  Topical Nano-Vesicular Spanlastics of Celecoxib: Enhanced Anti-Inflammatory Effect and Down-Regulation of TNF-α, NF-кB and COX-2 in Complete Freund's Adjuvant-Induced Arthritis Model in Rats.

Authors:  Eman Alaaeldin; Heba A Abou-Taleb; Soad A Mohamad; Mahmoud Elrehany; Shereen S Gaber; Heba F Mansour
Journal:  Int J Nanomedicine       Date:  2021-01-08

8.  Design and Evaluation of Ethyl Cellulose Based Matrix Tablets of Ibuprofen with pH Modulated Release Kinetics.

Authors:  S Chandran; Laila F A Asghar; Neelima Mantha
Journal:  Indian J Pharm Sci       Date:  2008-09       Impact factor: 0.975

9.  Estimation of intragastric solubility of drugs: in what medium?

Authors:  Maria Vertzoni; Eleni Pastelli; Dimitris Psachoulias; Lida Kalantzi; Christos Reppas
Journal:  Pharm Res       Date:  2007-03-20       Impact factor: 4.580

10.  Influence of sodium lauryl sulfate and tween 80 on carbamazepine-nicotinamide cocrystal solubility and dissolution behaviour.

Authors:  Mingzhong Li; Ning Qiao; Ke Wang
Journal:  Pharmaceutics       Date:  2013-10-11       Impact factor: 6.321

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.