Literature DB >> 21449826

Suitability of various excipients as carrier and coating materials for liquisolid compacts.

Christina M Hentzschel1, Albrecht Sakmann, Claudia S Leopold.   

Abstract

CONTEXT: The liquisolid technology is a promising technique for the release enhancement of poorly soluble drugs. With this approach, liquids such as solutions or suspensions of poorly soluble drugs in a non-volatile liquid vehicle are transformed into acceptably flowing and compressible powders. As fast-release liquisolid compacts require a high amount of liquid vehicle, more effective tableting excipients for liquid adsorption are needed to reduce tablet weight.
OBJECTIVE: The aim of this study was to investigate the suitability of various novel tableting excipients as carrier and coating materials for liquisolid compacts.
MATERIALS AND METHODS: Liquisolid compacts containing the liquid drug tocopherol acetate (TA) as model drug and various excipients were prepared. The effect of liquid drug content on the flowability and tabletability of the liquisolid powder blends as well as the disintegration of the liquisolid compacts was studied. From this data, the maximum liquid adsorption capacity of the respective mixtures of carrier and coating materials could be determined. RESULTS AND DISCUSSION: The liquid adsorption capacity depends on the specific surface area of the investigated excipients. Fujicalin(®) and especially Neusilin(®) are more effective carrier materials for liquid adsorption than Avicel(®), which is often used for liquisolid systems. Moreover, Florite(®) and Neusilin(®) turned out to be more suitable as coating materials than the commonly used Aerosil(®) due to their better tableting properties.
CONCLUSION: If Neusilin(®) is used as carrier and coating material instead of Avicel(®) (carrier material) and Aerosil(®) (coating material), the TA adsorption capacity is increased by a factor of 7.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21449826     DOI: 10.3109/03639045.2011.564184

Source DB:  PubMed          Journal:  Drug Dev Ind Pharm        ISSN: 0363-9045            Impact factor:   3.225


  19 in total

Review 1.  Transforming lipid-based oral drug delivery systems into solid dosage forms: an overview of solid carriers, physicochemical properties, and biopharmaceutical performance.

Authors:  Angel Tan; Shasha Rao; Clive A Prestidge
Journal:  Pharm Res       Date:  2013-06-18       Impact factor: 4.200

2.  First in man bioavailability and tolerability studies of a silica-lipid hybrid (Lipoceramic) formulation: a Phase I study with ibuprofen.

Authors:  Angel Tan; Nasrin Ghouchi Eskandar; Shasha Rao; Clive A Prestidge
Journal:  Drug Deliv Transl Res       Date:  2014-06       Impact factor: 4.617

3.  Development of Solid SEDDS, IV: Effect of Adsorbed Lipid and Surfactant on Tableting Properties and Surface Structures of Different Silicates.

Authors:  Suhas G Gumaste; Sara A Pawlak; Damon M Dalrymple; Charles J Nider; Louis D Trombetta; Abu T M Serajuddin
Journal:  Pharm Res       Date:  2013-06-26       Impact factor: 4.200

4.  Development of Solid SEDDS, V: Compaction and Drug Release Properties of Tablets Prepared by Adsorbing Lipid-Based Formulations onto Neusilin® US2.

Authors:  Suhas G Gumaste; Damon M Dalrymple; Abu T M Serajuddin
Journal:  Pharm Res       Date:  2013-06-25       Impact factor: 4.200

5.  Modern evaluation of liquisolid systems with varying amounts of liquid phase prepared using two different methods.

Authors:  Barbora Vraníková; Jan Gajdziok; David Vetchý
Journal:  Biomed Res Int       Date:  2015-05-17       Impact factor: 3.411

6.  Effect of hydrogen bond formation/replacement on solubility characteristics, gastric permeation and pharmacokinetics of curcumin by application of powder solution technology.

Authors:  Vijay Sharma; Kamla Pathak
Journal:  Acta Pharm Sin B       Date:  2016-06-14       Impact factor: 11.413

7.  Liquigroud technique: a new concept for enhancing dissolution rate of glibenclamide by combination of liquisolid and co-grinding technologies.

Authors:  Leila Azharshekoufeh; Javad Shokri; Mohammad Barzegar-Jalali; Yousef Javadzadeh
Journal:  Bioimpacts       Date:  2017-02-28

8.  Systematic Development of Self-Nanoemulsifying Liquisolid Tablets to Improve the Dissolution and Oral Bioavailability of an Oily Drug, Vitamin K1.

Authors:  Yongtao Tong; Yuli Wang; Meiyan Yang; Jiahui Yang; Lu Chen; Xiaoyang Chu; Chunhong Gao; Qian Jin; Wei Gong; Chunsheng Gao
Journal:  Pharmaceutics       Date:  2018-07-18       Impact factor: 6.321

9.  Liquisolid pellets: A pharmaceutical technology strategy to improve the dissolution rate of ritonavir.

Authors:  Brenda De Espíndola; André O'Reilly Beringhs; Diva Sonaglio; Hellen Karine Stulzer; Marcos Antônio Segatto Silva; Humberto Gomes Ferraz; Bianca Ramos Pezzini
Journal:  Saudi Pharm J       Date:  2019-04-03       Impact factor: 4.330

Review 10.  Pharmaceutical Dispersion Techniques for Dissolution and Bioavailability Enhancement of Poorly Water-Soluble Drugs.

Authors:  Xingwang Zhang; Huijie Xing; Yue Zhao; Zhiguo Ma
Journal:  Pharmaceutics       Date:  2018-06-23       Impact factor: 6.321

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.