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https://www.sciencedirect.com/science/article/pii/S0022354916325497
PLGA Nanoparticles for Oral Delivery of Hydrophobic Drugs: Influence of Organic Solvent on Nanoparticle Formation and Release Behavior In Vitro and In Vivo Using Estradiol as a Model DrugAuthor: D.K. Sahana, G. Mittal, V. Bhardwaj, M.N.V.Ravi Kumar
https://onlinelibrary.wiley.com/doi/full/10.1002/jps.21158
PLGA nanoparticles for oral delivery of hydrophobic drugs: Influence of organic solvent on nanoparticle formation and release behavior In Vitro and In Vivo using estradiol as a model drug D.K. Sahana. Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research (NIPER), S.A.S. Nagar 160 062, Punjab, India ...Author: D.K. Sahana, G. Mittal, V. Bhardwaj, M.N.V.Ravi Kumar
https://www.ncbi.nlm.nih.gov/pubmed/17722098
PLGA nanoparticles for oral delivery of hydrophobic drugs: influence of organic solvent on nanoparticle formation and release behavior in vitro and in vivo using estradiol as a model drug. Sahana DK(1), Mittal G, Bhardwaj V, Kumar MN.Author: D.K. Sahana, G. Mittal, V. Bhardwaj, M.N.V.Ravi Kumar
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3347861/
Sep 01, 2011 · In past two decades poly lactic-co-glycolic acid (PLGA) has been among the most attractive polymeric candidates used to fabricate devices for drug delivery and tissue engineering applications.PLGA is biocompatible and biodegradable, exhibits a wide range of erosion times, has tunable mechanical properties and most importantly, is a FDA approved polymer.Author: Hirenkumar K. Makadia, Steven J. Siegel
https://www.mdpi.com/2073-4360/11/10/1632/pdf
In many studies, using nanoparticles (NPs) as a drug delivery system has been shown to increase the e ectiveness and bioavailability of active drug substances. This study describes the development and evaluation of poly (lactic-co-glycolic acid) (PLGA) NPs and chitosan (CS)-coated PLGA NPs for oral delivery of CLR.Author: A. Alper Öztürk, Evrim Yenilmez, Mustafa Güçlü Özarda
https://www.researchgate.net/publication/313416618_PLGA_nanoparticles_for_the_oral_delivery_of_nuciferine_preparation_physicochemical_characterization_and_in_vitro_in_vivo_studies
PLGA nanoparticles for the oral delivery of nuciferine: preparation, physicochemical characterization and in vitro / in vivo studies. ... [21], especially for some highly hydrophobic drugs [22,23 ...
https://pubs.acs.org/doi/10.1021/mp200469a
We have designed a triple action nanomedicine from a chitosan amphiphile: quaternary ammonium palmitoyl glycol chitosan (GCPQ), which significantly enhances the oral absorption of hydrophobic drugs (e.g., griseofulvin and cyclosporin A) and, to a lesser extent, the absorption of hydrophilic drugs …Author: Adeline Siew, Hang Le, Marion Thiovolet, Paul Gellert, Andreas Schatzlein, Ijeoma Uchegbu
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0155710
Polymer nanoparticles are vehicles used for delivery of hydrophobic anti-cancer drugs, like doxorubicin, paclitaxel or chemopreventors like quercetin (Q). The present study deals with the synthesis and characterisation of nano formulations (NFs) from Q loaded PLGA (poly lactic-co-glycolic acid) nano particles (NPs) by surface modification.
https://www.degruyter.com/view/j/ntrev.2013.2.issue-3/ntrev-2012-0084/ntrev-2012-0084.xml?lang=en
Jun 01, 2013 · In this review, a literature search was conducted on the subject of PLGA/PLA NPs and brain delivery of drugs using PubMed, ScienceDirect and SpringerLink databases. The following keywords were used in the search: polymeric/PLGA nanoparticles, brain delivery, blood-brain barrier, central nervous system and neuron delivery.Author: Jingyan Li, Cristina Sabliov
https://strathprints.strath.ac.uk/13193/
Sahana, D.K. and Mittal, G. and Bhardwaj, V. and Kumar, M.N.V. Ravi () PLGA nanoparticles for oral delivery of hydrophobic drugs: influence of organic solvent on nanoparticle formation and release behavior in vitro and in vivo using estradiol as a model drug. Journal of Pharmaceutical Sciences, 97 (4).pp. 1530-1542. ISSN 0022-3549 Full text not available in this repository.Author: D.K. Sahana, G. Mittal, V. Bhardwaj, M.N.V.Ravi Kumar
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