Literature DB >> 16394546

Preparation and evaluation of solid dispersions of nitrendipine prepared with fine silica particles using the melt-mixing method.

Liang Wang1, Fu De Cui, Hisakazu Sunada.   

Abstract

Solid dispersions (SD) of nitrendipine (NTD), a poorly water-soluble drug, were prepared using the melt-mixing method with hydrophilic silica particles (Aerosil and Sylysia) with different particle size and specific surface areas as carriers. Powder X-ray diffraction and differential scanning calorimetry evaluation showed that NTD in the SDs treated with the melt-mixing method was dispersed in the amorphous state. FT-IR spectroscopy obtained with the SDs indicated the presence of hydrogen bonding between the secondary amine groups of NTD and silanol groups of silica particles. The dissolution property of NTD in the SDs was remarkably improved regardless of the grade of silica. At the end of the dissolution test (60 min) the concentrations of NTD for the SDs with Aerosil 200 and Sylysia 350 were 8.88 and 10.09 microg/ml, corresponding to 28 and 31 times that of the original NTD crystals, respectively. The specific surface area and the adsorbed water amount of the SDs were also significantly improved. The rapid dissolution rate from the SDs was attributed to the amorphization of drug, improved specific surface area and wettability than the original drug crystals. In the stability test, powder X-ray diffraction pattern indicated that amorphous NTD in the SD with Aerosil 200 was stable for at least 1 month under the humid conditions (40 degrees C/75% RH).

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Year:  2006        PMID: 16394546     DOI: 10.1248/cpb.54.37

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  10 in total

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Journal:  AAPS PharmSciTech       Date:  2008-04-09       Impact factor: 3.246

2.  Nitrendipine nanocrystals: its preparation, characterization, and in vitro-in vivo evaluation.

Authors:  Peng Quan; Dengning Xia; Hongze Piao; Hongyu Piao; Kai Shi; Yinnong Jia; Fude Cui
Journal:  AAPS PharmSciTech       Date:  2011-09-03       Impact factor: 3.246

3.  Elucidation of Compression-Induced Surface Crystallization in Amorphous Tablets Using Sum Frequency Generation (SFG) Microscopy.

Authors:  Pei T Mah; Dunja Novakovic; Jukka Saarinen; Stijn Van Landeghem; Leena Peltonen; Timo Laaksonen; Antti Isomäki; Clare J Strachan
Journal:  Pharm Res       Date:  2016-10-13       Impact factor: 4.200

4.  Development, optimization, and characterization of solid self-nanoemulsifying drug delivery systems of valsartan using porous carriers.

Authors:  Sarwar Beg; Suryakanta Swain; Harendra Pratap Singh; Ch Niranjan Patra; M E Bhanoji Rao
Journal:  AAPS PharmSciTech       Date:  2012-10-16       Impact factor: 3.246

5.  Evaluation of colloidal solid dispersions: physiochemical considerations and in vitro release profile.

Authors:  Vaibhav I Patel; Rutesh H Dave
Journal:  AAPS PharmSciTech       Date:  2013-03-15       Impact factor: 3.246

6.  Physicochemical investigations and stability studies of amorphous gliclazide.

Authors:  Shital Jondhale; Satish Bhise; Yogesh Pore
Journal:  AAPS PharmSciTech       Date:  2012-03-02       Impact factor: 3.246

7.  Amorphization alone does not account for the enhancement of solubility of drug co-ground with silicate: the case of indomethacin.

Authors:  Deepak Bahl; Robin H Bogner
Journal:  AAPS PharmSciTech       Date:  2008-01-19       Impact factor: 3.246

8.  Novel biodegradable polyester poly(propylene succinate): synthesis and application in the preparation of solid dispersions and nanoparticles of a water-soluble drug.

Authors:  Dimitrios N Bikiaris; George Z Papageorgiou; Sofia A Papadimitriou; Evangelos Karavas; Konstantinos Avgoustakis
Journal:  AAPS PharmSciTech       Date:  2009-02-04       Impact factor: 3.246

9.  Preparation, characterization, and in vivo evaluation of tanshinone IIA solid dispersions with silica nanoparticles.

Authors:  Yan-rong Jiang; Zhen-hai Zhang; Qi-yuan Liu; Shao-ying Hu; Xiao-yun Chen; Xiao-bin Jia
Journal:  Int J Nanomedicine       Date:  2013-06-25

Review 10.  Crosslinked hydrogels-a promising class of insoluble solid molecular dispersion carriers for enhancing the delivery of poorly soluble drugs.

Authors:  Dajun D Sun; Ping I Lee
Journal:  Acta Pharm Sin B       Date:  2014-01-22       Impact factor: 11.413

  10 in total

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