Literature DB >> 18096270

Challenges and opportunities in the encapsulation of liquid and semi-solid formulations into capsules for oral administration.

Ewart T Cole1, Dominique Cadé, Hassan Benameur.   

Abstract

The encapsulation of liquids and semi-solids provides solutions for convenient delivery through improved oral absorption of poorly water-soluble drugs. In addition, low dose (content uniformity), highly potent (containment), low melting point drugs, those with a critical stability profile and those for which a delayed release is required are candidates for liquid or semi-solid formulations. Both hard and soft capsules can be considered and in each case the capsule wall may comprise gelatin or some other suitable polymer such as hypromellose. The choice of a hard or soft capsule will depend primarily on the components of the formulation which provides the best absorption characteristics as well as on the physical characteristics, such as the viscosity of the formulation and the temperature at which the product needs to be filled. Numerous excipients are available for formulation of lipid-based systems and their compatibilities with hard gelatin capsules have been tested. The availability of new enhanced manufacturing equipment has brought new opportunities for liquid-filled hard capsules. Filling and sealing technologies for hard capsules, provides the formulator with the flexibility of developing formulations in-house from small scale, as required for Phase I studies, up to production.

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Year:  2007        PMID: 18096270     DOI: 10.1016/j.addr.2007.09.009

Source DB:  PubMed          Journal:  Adv Drug Deliv Rev        ISSN: 0169-409X            Impact factor:   15.470


  28 in total

1.  Spontaneous emulsification of nifedipine-loaded self-nanoemulsifying drug delivery system.

Authors:  Yotsanan Weerapol; Sontaya Limmatvapirat; Mont Kumpugdee-Vollrath; Pornsak Sriamornsak
Journal:  AAPS PharmSciTech       Date:  2014-10-31       Impact factor: 3.246

2.  The manufacture of low-dose oral solid dosage form to support early clinical studies using an automated micro-filing system.

Authors:  Mingda Bi; Changquan Calvin Sun; Francisco Alvarez; Fernando Alvarez-Nunez
Journal:  AAPS PharmSciTech       Date:  2010-12-23       Impact factor: 3.246

Review 3.  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

4.  Ordered nanoporous silica as carriers for improved delivery of water insoluble drugs: a comparative study between three dimensional and two dimensional macroporous silica.

Authors:  Ying Wang; Qinfu Zhao; Yanchen Hu; Lizhang Sun; Ling Bai; Tongying Jiang; Siling Wang
Journal:  Int J Nanomedicine       Date:  2013-10-22

5.  Self-nanoemulsifying drug delivery system of nifedipine: impact of hydrophilic-lipophilic balance and molecular structure of mixed surfactants.

Authors:  Yotsanan Weerapol; Sontaya Limmatvapirat; Jurairat Nunthanid; Pornsak Sriamornsak
Journal:  AAPS PharmSciTech       Date:  2014-01-23       Impact factor: 3.246

6.  Introduction of a theoretical splashing degree to assess the performance of low-viscosity oils in filling of capsules.

Authors:  Andreas Niederquell; Martin Kuentz
Journal:  AAPS PharmSciTech       Date:  2011-02-01       Impact factor: 3.246

7.  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

8.  Development of solid self-emulsifying drug delivery system (SEDDS) I: use of poloxamer 188 as both solidifying and emulsifying agent for lipids.

Authors:  Ankita V Shah; Abu T M Serajuddin
Journal:  Pharm Res       Date:  2012-02-28       Impact factor: 4.200

9.  Facile Preparation of Crosslinked Polymeric Nanocapsules via Combination of Surface-Initiated Atom Transfer Radical Polymerization and Ultraviolet Irradiated Crosslinking Techniques.

Authors:  Bin Mu; Ruoping Shen; Peng Liu
Journal:  Nanoscale Res Lett       Date:  2009-05-06       Impact factor: 4.703

10.  Porous magnesium aluminometasilicate tablets as carrier of a cyclosporine self-emulsifying formulation.

Authors:  Camilla Sander; Per Holm
Journal:  AAPS PharmSciTech       Date:  2009-11-20       Impact factor: 3.246

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