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http://www.bioline.org.br/pdf?pr08028
Multiparticulate Drug Delivery Systems for Controlled Release NS Dey*, S Majumdar and MEB Rao Department of Pharmaceutics, Roland Institute of Pharmaceutical Sciences, Khodasinghi, Berhampur, Orissa760010, India Abstract Pharmaceutical invention and research are increasingly focusing on delivery systems which enhance
https://www.tandfonline.com/doi/pdf/10.1517/17425247.2016.1166203
EDITORIAL Micro/nano-particulate drug delivery systems: a boon for the treatment of inflammatory bowel disease Mayur M. Patel Department of Pharmaceutics, Nirma University, Institute of Pharmacy, Ahmedabad, IndiaAuthor: Mayur M. Patel
https://www.sciencedirect.com/science/article/pii/S0168365917310325
There is progressive evolution in the use of inhalable drug delivery systems (DDSs) for lung cancer therapy. The inhalation route offers many advantages, being non-invasive method of drug administration as well as localized delivery of anti-cancer drugs to tumor tissue.Author: Hadeer M. Abdelaziz, Mohamed Gaber, Mahmoud M. Abd-Elwakil, Moustafa T. Mabrouk, Mayada M. Elgohary,...
https://www.pharma-iq.com/pre-clinical-discovery-and-development/articles/multiparticulate-drug-delivery-systems
Most of the multiparticulate systems available in market are present in the form of capsules. If they are compressed in to tablets, the coating may be removed or the release rate may be altered. Elan drug technologies, U.S. intoduced multiparticulate drug delivery systems technologies as SODAS®, IPDAS®, and PRODAS® .
https://www.ncbi.nlm.nih.gov/pubmed/29180168
Jan 10, 2018 · The active targeting approaches for enhanced delivery of nanocarriers to lung cancer cells were illustrated. This article also reviews the recent advances of inhalable microparticle-based drug delivery systems for lung cancer therapy including bioresponsive, large porous, solid lipid and drug-complex microparticles.Author: Hadeer M. Abdelaziz, Mohamed Gaber, Mahmoud M. Abd-Elwakil, Moustafa T. Mabrouk, Mayada M. Elgohary,...
https://www.sciencedirect.com/topics/materials-science/particulate-system
Particulate systems made of natural and synthetic polymers or other biomaterials offer great advantages in diverse regenerative medicine and drug delivery applications [206–208]. The difference in size entails real differences, at many levels, from formulation to clinical performance.
http://www.aspbs.com/drug.htm
Handbook of Particulate Drug Delivery is an attempt to bring together, under a single cover, the promising aspects of nano- and micro-particulate materials dealing with their chemistry, biology, engineering, and their medical aspects. This work is the first ever published in this research area that draws on past decades of pioneering research ...
https://www.icevirtuallibrary.com/doi/10.1680/jbibn.16.00039
Jun 20, 2018 · In the recent progressive scientific era, lipid particulate drug delivery systems (LPDDSs) have been developed to furnish targeted and controlled release of drugs with variable molecular weight.1 Biopharmaceutics Classification System (BCS) class II and IV drugs are challenging for researchers in terms of bioavailability and solubility.2 Efficient size-dependent characteristics have been ...Author: IjazHira, QureshiJunaid, TulainUme Ruqia, IqbalFurqan, DanishZeeshan, FayyazAhad, SethiAyesha
https://www.free-ebooks.net/reference/Drug-Delivery-Systems-A-Review/pdf?dl&preview
This field of drug delivery systems is dynamic and extensive. Probably it would need an encyclopedia to cover all the types of drug delivery systems. The aim of this book is to compile major drug delivery systems and offer a source of information for all those working …
http://www.pharmtech.com/multiunit-particulate-systems-current-drug-delivery-technology
Jul 02, 2011 · Multiunit particulate systems (MUPS) are a novel MDDS technique for controlled and modified drug delivery. MUPS offer various advantages over other systems, including reduced risk of local irritation and toxicity, predictable bioavailability, reduced likelihood of dose dumping, minimized fluctuations in plasma concentration of drug, and high dose-strength administration (1).
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