50 Synthesis, characterization and stability of five tavaborole-based pharmaceutical cocrystals. (19th December 2016)
- Record Type:
- Journal Article
- Title:
- 50 Synthesis, characterization and stability of five tavaborole-based pharmaceutical cocrystals. (19th December 2016)
- Main Title:
- 50 Synthesis, characterization and stability of five tavaborole-based pharmaceutical cocrystals
- Authors:
- Zhang, Xiaoming
Song, Jialong
Xie, Peng
Guo, Xiufen
Meng, Fanxin - Abstract:
- Abstract : Objectives: Pharmaceutical cocrystals have received attention in the pharmaceutical industry due to their potential for readily changing the physicochemical and biological properties of free active pharmaceutical ingredients (API). Tavaborole is an antifungal agent with strong moisture absorption leading to poor stability. The objective of this investigation was to prepare five pharmaceutical tavaborole cocrystals and to optimize their stability. Methods: The five novel pharmaceutical cocrystals with tavaborole as the API were synthesised using the grinding method, with p-aminobenzoic acid (cocrystal 1), m-aminobenzoic acid (cocrystal 2), 2, 3'-dihydroxybenzoic acid (cocrystal 3), salicylic acid (cocrystal 4) and 2, 6'-pyridinedicarboxylic acid (cocrystal 5). Characterization with XRD and TGA further identified a new phase. The thermal stability, chemical stability and moisture absorption rate of API and cocrystals were also measured and discussed. Results: The thermal stability of the five cocrystals was significantly improved compared to the API alone. Chemical degradation and a hydration reaction of cocrystals did not occur in 43%, 58%, 75% and 92% relative humidity at 25°C. The moisture absorption rate of API and cocrystals decreased in the order: API>cocrystal 2>cocrystal 1>cocrystal 4>cocrystal 3>cocrystal 5. Conclusions: In this study, we used the grinding method to synthesize pharmaceutical cocrystals of tavaborole. The thermal stability, chemicalAbstract : Objectives: Pharmaceutical cocrystals have received attention in the pharmaceutical industry due to their potential for readily changing the physicochemical and biological properties of free active pharmaceutical ingredients (API). Tavaborole is an antifungal agent with strong moisture absorption leading to poor stability. The objective of this investigation was to prepare five pharmaceutical tavaborole cocrystals and to optimize their stability. Methods: The five novel pharmaceutical cocrystals with tavaborole as the API were synthesised using the grinding method, with p-aminobenzoic acid (cocrystal 1), m-aminobenzoic acid (cocrystal 2), 2, 3'-dihydroxybenzoic acid (cocrystal 3), salicylic acid (cocrystal 4) and 2, 6'-pyridinedicarboxylic acid (cocrystal 5). Characterization with XRD and TGA further identified a new phase. The thermal stability, chemical stability and moisture absorption rate of API and cocrystals were also measured and discussed. Results: The thermal stability of the five cocrystals was significantly improved compared to the API alone. Chemical degradation and a hydration reaction of cocrystals did not occur in 43%, 58%, 75% and 92% relative humidity at 25°C. The moisture absorption rate of API and cocrystals decreased in the order: API>cocrystal 2>cocrystal 1>cocrystal 4>cocrystal 3>cocrystal 5. Conclusions: In this study, we used the grinding method to synthesize pharmaceutical cocrystals of tavaborole. The thermal stability, chemical stability and hygroscopic stability of cocrystals were significantly better than those of API alone. Acknowledgments: We are grateful to the Major International (Regional) Joint Research Project of NSFC (Grant No. 21120102034). … (more)
- Is Part Of:
- Journal of investigative medicine. Volume 64(2016)Supplement 8
- Journal:
- Journal of investigative medicine
- Issue:
- Volume 64(2016)Supplement 8
- Issue Display:
- Volume 64, Issue 8 (2016)
- Year:
- 2016
- Volume:
- 64
- Issue:
- 8
- Issue Sort Value:
- 2016-0064-0008-0000
- Page Start:
- A18
- Page End:
- A18
- Publication Date:
- 2016-12-19
- Subjects:
- Clinical medicine -- Periodicals
Medicine -- Research -- Periodicals
Medicine
Research -- United States
Clinical medicine
Medicine -- Research
Periodicals
616.075 - Journal URLs:
- http://journals.lww.com/jinvestigativemed/pages/default.aspx ↗
http://jim.bmj.com/ ↗
https://journals.sagepub.com/home/IMJ ↗
http://journals.lww.com ↗ - DOI:
- 10.1136/jim-2016-000328.50 ↗
- Languages:
- English
- ISSNs:
- 1081-5589
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5008.010000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 18654.xml