We have collected information about Lipid Microspheres As Drug Delivery Systems for you. Follow the links to find out details on Lipid Microspheres As Drug Delivery Systems.
https://www.researchgate.net/publication/281545558_Lipid_microspheres_as_drug_delivery_systems
Lipid nanospheres (LN) are simple colloidal drug delivery systems, which are proven to be useful for the systemic delivery of lipophilic anticancer drugs.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241619/
To resolve these issues, lipid microspheres, often called lipospheres, have been proposed as a new type of fat-based encapsulation system for drug delivery of bioactive compounds. Lipospheres are lipid based water dispersible solid particles bearing particle size between 0.01 and 100 μm in diameter,...
https://www.sciencedirect.com/science/article/pii/0169409X9500114M
Liposomes are excellent drug carrier vehicles for Drug Delivery Systems (DDS) [1-3]. However, liposomes are relatively unstable and are not easily mass-produced. Lipid microspheres, with an average diameter of 0.2 /Jim, and consisting of soybean oil and lecithin (Fig. 1), however, are widely used in clinical medicine for parenteral nutrition (intralipid, 0169-409X/96/$32.00 1996 Eisevier Science B.V.Author: Yutaka Mizushima
https://www.sciencedirect.com/science/article/abs/pii/0169409X9500115N
The lipid microsphere (LM) formulation (Lipo-PGE 1) of prostaglandin E 1 (PGE 1) is an excellent pharmaceutical with a high degree of clinical efficacy. This review describes, from the pharmaceutical point of view, an attempt to clarify the physicochemical properties of LM for injection.Author: Tetsuo Yamaguchi
https://www.sciencedirect.com/science/article/pii/0169409X9500115N
Considering these problems, the lipid microsphere (LM), formed by dispersion of the LM particles in aqueous solution, appears to be a safe and excellent drug carrier [12-18]. Since LM was first used as a DDS pharma- ceutical around 1970, Jeppsson applied it to barbituric acid [19], and further applications to nitroglycerin and cyclandelate [20] were ex- amined [21].Author: Tetsuo Yamaguchi
https://www.jgtps.com/admin/uploads/YqxI0h.pdf
Adhesion of drug delivery device to the mucosal membrane such as buccal, ocular, rectal, nasal etc can be termed as bio adhesion. These kinds of microspheres exhibit a prolonged residence time at the site of application and causes intimate contact with the …File Size: 1MB
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