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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040871/
Proliposomes exhibited superior stability as compared to liposomes and it offers non-invasive delivery of drug into or across the skin. Since better stability of liposomes in vitro is observed with proliposomes, the proliposomes would be proper choice of preparation method.
https://www.sciencedirect.com/science/article/pii/S0928098714003170
In the present study, Proliposomes were studied as a drug delivery system to decrease hepatic first-pass metabolism. Lovastatin was chosen as the model drug. 3.1. Formulation of proliposomes. SPC, HEPC and DMPG were the three lipids used in the present investigation.Author: Sarala Yanamandra, Natarajan Venkatesan, Veeran Gowda Kadajji, Zhijun Wang, Manish Issar, Guru V. Be...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581684/
Proliposomes were capable of forming a liposomal suspension upon the addition of a water phase or in vivo conditions . They offer the opportunity to form liposomes only at the site of delivery, which is more stable during sterilization and storage. Proliposomes are defined as dry, free-flowing particles at first . Liquid proliposomes were developed in recent years.Author: Chuandi Sun, Ji Wang, Jianping Liu, Lu Qiu, Wenli Zhang, Lei Zhang
https://www.semanticscholar.org/paper/Proliposomes-as-Pharmaceutical-Drug-Delivery-A-Muneer-Masood/5b3ab9f3fd3ff396ed48c681ae49dfbf103fcc7e
Liposomes, the microscopic vesicles, are composed of a bilayer of phospholipids and a novel drug delivery system that provides drug at predetermined rate decided according to need, pharmacological aspects, drug profile, physiological conditions of body etc. But liposomes exhibit poor stability problem and this leads to their storage problem.
https://www.semanticscholar.org/paper/Proliposomes-as-Pharmaceutical-Drug-Delivery-A-Muneer-Masood/e744baac68264ad5431f270c42c88fe289349143
Liposomes, the microscopic vesicles, are composed of a bilayer of phospholipids and a novel drug delivery system that provides drug at predetermined rate decided according to need, pharmacological aspects, drug profile, physiological conditions of body etc. But liposomes exhibit poor stability problem and this leads to their storage problem.
http://ijrpns.com/article/PROLIPOSOMES%20AS%20A%20NOVEL%20DRUG%20DELIVERY%20SYSTEM%20FOR%20THE%20IMPROVEMENT%20OF%20VESICULAR%20STABILITY.pdf
Liposomes are the most promising and broadly applicable of all the novel drug delivery systems.
https://www.omicsonline.org/open-access/liposomes-for-drug-delivery-2155-952X276-97370.html
Liposomes are a novel drug delivery system (NDDS), they are vesicular structures consisting of bilalyers which form spontaneously when phospholipids are dispersed in water. They are microscopic vesicles in which an aqueous volume is entirely enclosed by a membrane composed of lipid bilayers.Author: Durgavati Yadav, Kumar Sandeep, Deepak Pandey, Ranu Kumari Dutta
https://www.sciencedirect.com/science/article/pii/S2211383517307311
The practice of developing liposomes as oral drug delivery systems has motivated investigations on the mass production of liposomes on an industrial scale. On a laboratory scale, liposomes can be prepared using a variety of methods such as thin-film dispersion, reversed-phase evaporation, detergent dialysis, solvent injection and a few other methods 154 .Author: Haisheng He, Yi Lu, Jianping Qi, Quangang Zhu, Zhongjian Chen, Wei Wu
https://www.researchgate.net/publication/281063035_Liposomes_as_a_Drug_Delivery_System
The discovery of phospholipids spontaneously forming spherical, self-closed bubbles known as liposomes, upon dispersion in water, ushered a new era in drug delivery technology.
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