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Ji Wang

Researcher at China Pharmaceutical University

Publications -  7
Citations -  193

Ji Wang is an academic researcher from China Pharmaceutical University. The author has contributed to research in topics: Nanocarriers & Nimodipine. The author has an hindex of 6, co-authored 7 publications receiving 166 citations. Previous affiliations of Ji Wang include Fourth Military Medical University.

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Pharmacokinetics and atherosclerotic lesions targeting effects of tanshinone IIA discoidal and spherical biomimetic high density lipoproteins.

TL;DR: In this paper, Discoidal and spherical recombinant HDL loaded with cardiovascular drug tanshinone IIA (TA) were constructed (TA-d-rHDL and TA-s-RHDL), and their in vitro physiochemical and biomimetic properties were characterized.
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Tumor targeting effects of a novel modified paclitaxel-loaded discoidal mimic high density lipoproteins

TL;DR: In this article, the authors developed a novel biomimetic nanocarriers that were developed for tumor targeting delivery to avoid unexpected drug leakage from discoidal reconstituted high density lipoproteins (d-rHDL) during remodeling process associated with lecithin-cholesterol acyltransferase (LCAT).
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Liquid Proliposomes of Nimodipine Drug Delivery System: Preparation, Characterization, and Pharmacokinetics

TL;DR: NPSC offered a potential way to improve oral delivery of nimodipine and presented similar pharmacokinetic parameters compared with NPSC.
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Arachidonic acid-modified lovastatin discoidal reconstituted high density lipoprotein markedly decreases the drug leakage during the remodeling behaviors induced by lecithin cholesterol acyltransferase.

TL;DR: With increment of AA modification amount, AA-LT-d-rHDL manifested lower reactivity with LCAT, thus significantly reducing the undesired drug leakage during the remodeling behaviors induced by LCAT.
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A Simple Method to Extract Whole Apolipoproteins for the Preparation of Discoidal Recombined High Density Lipoproteins as Bionic Nanocarriers for Drug Delivery.

TL;DR: Sterol efflux assay from macrophages mediated by TA-rHDLs and structure remodeling behavior from discs to spheres proved that TA- rHDL could resemble the biological activity of native nascent HDL irrespective of the size.