Literature DB >> 9756777

Use of microsphere technology for targeted delivery of rifampin to Mycobacterium tuberculosis-infected macrophages.

E L Barrow1, G A Winchester, J K Staas, D C Quenelle, W W Barrow.   

Abstract

Microsphere technology was used to develop formulations of rifampin for targeted delivery to host macrophages. These formulations were prepared by using biocompatible polymeric excipients of lactide and glycolide copolymers. Release characteristics were examined in vitro and also in two monocytic cell lines, the murine J774 and the human Mono Mac 6 cell lines. Bioassay assessment of cell culture supernatants from monocyte cell lines showed release of bioactive rifampin during a 7-day experimental period. Treatment of Mycobacterium tuberculosis H37Rv-infected monocyte cell lines with rifampin-loaded microspheres resulted in a significant decrease in numbers of CFU at 7 days following initial infection, even though only 8% of the microsphere-loaded rifampin was released. The levels of rifampin released from microsphere formulations within monocytes were more effective at reducing M. tuberculosis intracellular growth than equivalent doses of rifampin given as a free drug. These results demonstrate that rifampin-loaded microspheres can be formulated for effective sustained and targeted delivery to host macrophages.

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Year:  1998        PMID: 9756777      PMCID: PMC105919     

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  31 in total

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Journal:  J Infect Dis       Date:  1987-09       Impact factor: 5.226

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Journal:  Am Rev Respir Dis       Date:  1974-12

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Journal:  Tubercle       Date:  1984-06

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Authors:  D R Cowsar; T R Tice; R M Gilley; J P English
Journal:  Methods Enzymol       Date:  1985       Impact factor: 1.600

6.  Rationale for and efficacy of prolonged-interval treatment using liposome-encapsulated amikacin in experimental Mycobacterium avium infection.

Authors:  S Leitzke; W Bucke; K Borner; R Müller; H Hahn; S Ehlers
Journal:  Antimicrob Agents Chemother       Date:  1998-02       Impact factor: 5.191

7.  Long-acting delivery systems for peptides: inhibition of rat prostate tumors by controlled release of [D-Trp6]luteinizing hormone-releasing hormone from injectable microcapsules.

Authors:  T W Redding; A V Schally; T R Tice; W E Meyers
Journal:  Proc Natl Acad Sci U S A       Date:  1984-09       Impact factor: 11.205

8.  The use of rifampicin and isoniazid entrapped in liposomes for the treatment of Murine tuberculosis.

Authors:  L C Orozco; F O Quintana; R M Beltrán; I de Moreno; M Wasserman; G Rodriguez
Journal:  Tubercle       Date:  1986-06

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Authors:  M A Vladimirsky; G A Ladigina
Journal:  Biomed Pharmacother       Date:  1982       Impact factor: 6.529

10.  Biodegradation of and tissue reaction to 50:50 poly(DL-lactide-co-glycolide) microcapsules.

Authors:  G E Visscher; R L Robison; H V Maulding; J W Fong; J E Pearson; G J Argentieri
Journal:  J Biomed Mater Res       Date:  1985-03
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  21 in total

1.  Treatment of tuberculosis using a combination of sustained-release rifampin-loaded microspheres and oral dosing with isoniazid.

Authors:  D C Quenelle; G A Winchester; J K Staas; E L Barrow; W W Barrow
Journal:  Antimicrob Agents Chemother       Date:  2001-06       Impact factor: 5.191

2.  Respirable PLGA microspheres containing rifampicin for the treatment of tuberculosis: manufacture and characterization.

Authors:  P O'Hara; A J Hickey
Journal:  Pharm Res       Date:  2000-08       Impact factor: 4.200

3.  Efficacy of microencapsulated rifampin in Mycobacterium tuberculosis-infected mice.

Authors:  D C Quenelle; J K Staas; G A Winchester; E L Barrow; W W Barrow
Journal:  Antimicrob Agents Chemother       Date:  1999-05       Impact factor: 5.191

Review 4.  Nanoparticle delivery of anti-tuberculosis chemotherapy as a potential mediator against drug-resistant tuberculosis.

Authors:  Jonathan Paul Smith
Journal:  Yale J Biol Med       Date:  2011-12

Review 5.  The potential advantages of nanoparticle drug delivery systems in chemotherapy of tuberculosis.

Authors:  Svetlana Gelperina; Kevin Kisich; Michael D Iseman; Leonid Heifets
Journal:  Am J Respir Crit Care Med       Date:  2005-09-08       Impact factor: 21.405

6.  25-Hydroxyvitamin D(3)-loaded PLA microspheres: in vitro characterization and application in diabetic periodontitis models.

Authors:  Hao Li; Qi Wang; Yu Xiao; Chongyun Bao; Wei Li
Journal:  AAPS PharmSciTech       Date:  2013-05-08       Impact factor: 3.246

7.  Respirable PLGA microspheres containing rifampicin for the treatment of tuberculosis: screening in an infectious disease model.

Authors:  S Suarez; P O'Hara; M Kazantseva; C E Newcomer; R Hopfer; D N McMurray; A J Hickey
Journal:  Pharm Res       Date:  2001-09       Impact factor: 4.200

Review 8.  Current development and future prospects in chemotherapy of tuberculosis.

Authors:  Eric L Nuermberger; Melvin K Spigelman; Wing Wai Yew
Journal:  Respirology       Date:  2010-06-04       Impact factor: 6.424

9.  Formation of inhalable rifampicin-poly(L-lactide) microparticles by supercritical anti-solvent process.

Authors:  Vipaluk Patomchaiviwat; Ornlaksana Paeratakul; Poj Kulvanich
Journal:  AAPS PharmSciTech       Date:  2008-11-07       Impact factor: 3.246

10.  Slow release formulations of inhaled rifampin.

Authors:  Intira Coowanitwong; Vikram Arya; Poj Kulvanich; Günther Hochhaus
Journal:  AAPS J       Date:  2008-06-27       Impact factor: 4.009

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