Literature DB >> 12927382

Fluorescence and electron microscopy probes for cellular and tissue uptake of poly(D,L-lactide-co-glycolide) nanoparticles.

Jayanth Panyam1, Sanjeeb K Sahoo, Swayam Prabha, Tom Bargar, Vinod Labhasetwar.   

Abstract

Nanoparticles formulated from poly(D,L-lactide-co-glycolide) (PLGA) and poly(lactide) (PLA) are being extensively investigated for different therapeutic applications such as for sustained drug, vaccine, and gene delivery. For many of these applications, it is necessary to study the intracellular distribution as well as the tissue uptake of nanoparticles to optimize the efficacy of the encapsulated therapeutic agent. Fluorescence and electron microscopic techniques are usually used for the above purposes. Colloidal gold particles and fluorescent polystyrene, which are generally used as model particles for electron and fluorescence microscopy, respectively, may not be suitable alternatives to PLGA/PLA nanoparticles for these studies mainly because of the differences in their physical properties and also because they do not contain any therapeutic agent. The aim of the present study was to develop and characterize PLGA nanoparticle formulations that would be suitable for confocal/fluorescence and transmission electron microscopic (TEM) studies. Towards this objective, PLGA nanoparticles containing 6-coumarin as a fluorescent marker and osmium tetroxide as an electron microscopic marker with bovine serum albumin (BSA) as a model protein were formulated. Different physical properties of marker-loaded nanoparticles such as particle size, zeta potential, residual PVA content and protein-loading were compared with those of unloaded nanoparticles and were found to be not significantly different. Furthermore, marker-loaded nanoparticle formulations were non-toxic to the cells as unloaded nanoparticles. Nanoparticles loaded with 6-coumarin were found to be useful for studying intracellular nanoparticle uptake and distribution using confocal microscopy while osmium tetroxide-loaded nanoparticles were found to be useful for studying nanoparticle uptake and distribution in cells and tissue using TEM. It was concluded that 6-coumarin and osmium tetroxide could serve as useful fluorescence and electron microscopy probes, respectively, for incorporation into nanoparticles to study their cellular and tissue distribution.

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Year:  2003        PMID: 12927382     DOI: 10.1016/s0378-5173(03)00295-3

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


  54 in total

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Authors:  Serguei V Vinogradov; Ekta Kohli; Arin D Zeman
Journal:  Mol Pharm       Date:  2005 Nov-Dec       Impact factor: 4.939

Review 3.  Development of topical microbicides to prevent the sexual transmission of HIV.

Authors:  Robert W Buckheit; Karen M Watson; Kathleen M Morrow; Anthony S Ham
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4.  Kinetic analysis of nanoparticulate polyelectrolyte complex interactions with endothelial cells.

Authors:  Sean M Hartig; Rachel R Greene; Gianluca Carlesso; James N Higginbotham; Wasif N Khan; Ales Prokop; Jeffrey M Davidson
Journal:  Biomaterials       Date:  2007-05-03       Impact factor: 12.479

5.  Targeted delivery of antibiotics to intracellular chlamydial infections using PLGA nanoparticles.

Authors:  Udaya S Toti; Bharath R Guru; Mirabela Hali; Christopher M McPharlin; Susan M Wykes; Jayanth Panyam; Judith A Whittum-Hudson
Journal:  Biomaterials       Date:  2011-06-08       Impact factor: 12.479

6.  EILDV-conjugated, etoposide-loaded biodegradable polymeric micelles directing to tumor metastatic cells overexpressing α4β1 integrin.

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Journal:  Cancer Nanotechnol       Date:  2011-09-15

7.  Rhodamine-loaded poly(lactic-co-glycolic acid) nanoparticles for investigation of in vitro interactions with breast cancer cells.

Authors:  Tania Betancourt; Kunal Shah; Lisa Brannon-Peppas
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Review 8.  Nanovehicular intracellular delivery systems.

Authors:  Ales Prokop; Jeffrey M Davidson
Journal:  J Pharm Sci       Date:  2008-09       Impact factor: 3.534

9.  Selective biophysical interactions of surface modified nanoparticles with cancer cell lipids improve tumor targeting and gene therapy.

Authors:  Blanka Sharma; Chiranjeevi Peetla; Isaac M Adjei; Vinod Labhasetwar
Journal:  Cancer Lett       Date:  2013-03-21       Impact factor: 8.679

Review 10.  Nanoparticle-based targeted drug delivery.

Authors:  Rajesh Singh; James W Lillard
Journal:  Exp Mol Pathol       Date:  2009-01-07       Impact factor: 3.362

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