Literature DB >> 20429826

Aqueous solubility of crystalline and amorphous drugs: Challenges in measurement.

Sharad B Murdande1, Michael J Pikal, Ravi M Shanker, Robin H Bogner.   

Abstract

Measurement of drug solubility is one of the key elements of active pharmaceutical ingredient (API) characterization during the drug discovery and development process. This report is a critical review of experimental methods reported in the literature for the measurement of aqueous solubility of amorphous, partially crystalline and crystalline organic compounds. A summary of high-throughput automated methods used in early drug discovery research is also provided in this report. This review summarizes the challenges that are encountered during solubility measurement and the complexities that are often overlooked. Even though there is an advantage in using the amorphous form of a drug due to its higher solubility, measurement of its solubility with useful accuracy is still a practical problem. Therefore, this review provides recommendations of preferred methods and precautions in using these methods to determine the aqueous solubility of amorphous and crystalline new molecular entities, with emphasis on the physico-chemical characterization of the solid state of the test substance.

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Year:  2010        PMID: 20429826     DOI: 10.3109/10837451003774377

Source DB:  PubMed          Journal:  Pharm Dev Technol        ISSN: 1083-7450            Impact factor:   3.133


  17 in total

1.  Solubility at the molecular level: development of a critical aggregation concentration (CAC) assay for estimating compound monomer solubility.

Authors:  Jie Wang; Edmund Matayoshi
Journal:  Pharm Res       Date:  2012-03-16       Impact factor: 4.200

2.  Solubility advantage of amorphous pharmaceuticals: II. Application of quantitative thermodynamic relationships for prediction of solubility enhancement in structurally diverse insoluble pharmaceuticals.

Authors:  Sharad B Murdande; Michael J Pikal; Ravi M Shanker; Robin H Bogner
Journal:  Pharm Res       Date:  2010-09-22       Impact factor: 4.200

3.  Multi-channel GCN ensembled machine learning model for molecular aqueous solubility prediction on a clean dataset.

Authors:  Chenglong Deng; Li Liang; Guomeng Xing; Yi Hua; Tao Lu; Yanmin Zhang; Yadong Chen; Haichun Liu
Journal:  Mol Divers       Date:  2022-06-23       Impact factor: 2.943

4.  Pharmacotechnical Evaluation by SeDeM Expert System to Develop Orodispersible Tablets.

Authors:  Monica R P Rao; Sharwari Sapate; Ashwini Sonawane
Journal:  AAPS PharmSciTech       Date:  2022-05-09       Impact factor: 3.246

Review 5.  Lipid-based emulsion drug delivery systems - a comprehensive review.

Authors:  Mori Dhaval; Poonam Vaghela; Kajal Patel; Keshvi Sojitra; Mohini Patel; Sushma Patel; Kiran Dudhat; Sunny Shah; Ravi Manek; Ramesh Parmar
Journal:  Drug Deliv Transl Res       Date:  2021-10-05       Impact factor: 4.617

6.  A novel method for determining the solubility of small molecules in aqueous media and polymer solvent systems using solution calorimetry.

Authors:  Hala M Fadda; Xin Chen; Aktham Aburub; Dinesh Mishra; Rodolfo Pinal
Journal:  Pharm Res       Date:  2014-02-20       Impact factor: 4.200

7.  Image-based dissolution analysis for tracking the surface stability of amorphous powders.

Authors:  Jernej Štukelj; Mikael Agopov; Jouko Yliruusi; Clare J Strachan; Sami Svanbäck
Journal:  ADMET DMPK       Date:  2020-07-13

Review 8.  Efficacy and safety of turmeric and curcumin in lowering blood lipid levels in patients with cardiovascular risk factors: a meta-analysis of randomized controlled trials.

Authors:  Si Qin; Lifan Huang; Jiaojiao Gong; Shasha Shen; Juan Huang; Hong Ren; Huaidong Hu
Journal:  Nutr J       Date:  2017-10-11       Impact factor: 3.271

9.  Direct Measurement of Amorphous Solubility.

Authors:  Jernej Štukelj; Sami Svanbäck; Mikael Agopov; Korbinian Löbmann; Clare J Strachan; Thomas Rades; Jouko Yliruusi
Journal:  Anal Chem       Date:  2019-05-14       Impact factor: 6.986

Review 10.  Polymorph Impact on the Bioavailability and Stability of Poorly Soluble Drugs.

Authors:  Roberta Censi; Piera Di Martino
Journal:  Molecules       Date:  2015-10-15       Impact factor: 4.411

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