Literature DB >> 15814241

Cubic liquid crystalline glyceryl monooleate matrices for oral delivery of enzyme.

Manish H Shah1, Anant Paradkar.   

Abstract

In situ cubic phase transforming system of glyceryl monooleate (GMO) has been prepared which offers protection to the metaloenzyme, seratiopeptidase (STP), in gastric environment and provides delayed and controlled release with no initial burst after oral administration. Effect of magnesium trisilicate (MTS) on floating, proteolytic activity and drug release was studied. Gelucire 43/01 was incorporated in the system to provide prolonged lag time. The drug-loaded matrices required 100 mg of MTS to overcome floatability of GMO matrix. Plain GMO matrices showed 85.3% loss of proteolytic activity in acidic medium, whereas matrices containing MTS showed retention of activity (111.6%). The hydrophobic nature of MTS induced formation of cubic phase at faster rate and the existence of cubic phase was confirmed by polarizing light microscopy. Furthermore, MTS provided alkaline microenvironment, which prevented acid-catalyzed hydrolysis and protein unfolding. The magnesium ions restored the activity of STP. The release of STP was decreased with increasing amount of MTS in the matrix. Gelucire did not affect proteolytic activity. The water uptake of matrices with gelucire was decelerated due to formation of hexagonal phase. However, the rate of STP release from these matrices was very slow due to incorporation of gelucire into lipid bilayers, which provided resistance to movement of STP. Thus, microenvironment-controlled in situ cubic phase transforming GMO matrices provided protection to STP and controlled release.

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Year:  2005        PMID: 15814241     DOI: 10.1016/j.ijpharm.2005.01.019

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  13 in total

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Journal:  AAPS PharmSciTech       Date:  2006-09-15       Impact factor: 3.246

2.  Preparation and characterization of pluronic-colloidal silicon dioxide composite particles as liquid crystal precursor.

Authors:  Manish Maheshwari; Anant Paradkar; Shigeo Yamamura; Shivajirao Kadam
Journal:  AAPS PharmSciTech       Date:  2006       Impact factor: 3.246

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Journal:  AAPS PharmSciTech       Date:  2011-09-23       Impact factor: 3.246

5.  Nanostructured reverse hexagonal liquid crystals sustain plasma concentrations for a poorly water-soluble drug after oral administration.

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Authors:  Sharvil S Patil; Edakkal Venugopal; Suresh Bhat; Kakasaheb R Mahadik; Anant R Paradkar
Journal:  AAPS PharmSciTech       Date:  2015-02-26       Impact factor: 3.246

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Journal:  Indian J Pharm Sci       Date:  2010-01       Impact factor: 0.975

8.  Self-Assembled Cubic Liquid Crystalline Nanoparticles for Transdermal Delivery of Paeonol.

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9.  Serratiopeptidase Niosomal Gel with Potential in Topical Delivery.

Authors:  Ujwala A Shinde; Shivkumar S Kanojiya
Journal:  J Pharm (Cairo)       Date:  2014-03-20

10.  In vitro and in vivo evaluation of cubosomes containing 5-fluorouracil for liver targeting.

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Journal:  Acta Pharm Sin B       Date:  2014-12-29       Impact factor: 11.413

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