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dc.contributor.authorSandhiya, V.vi
dc.contributor.otherUbaidulla, U.vi
dc.date.accessioned2023-03-30T08:16:56Z-
dc.date.available2023-03-30T08:16:56Z-
dc.date.issued2022-
dc.identifier.issn2522-8307vi
dc.identifier.urihttp://tailieuso.tlu.edu.vn/handle/DHTL/12790-
dc.description.abstractOptimization of formulation factors of gallic acid-loaded PLGA nanoparticles is represented in Table 1, and the study was designed to determine the effects of three factors: (A; X1) lipid concentration, (B; X2) PLGA polymer concentration, and (C; X3) gallic acid concentration. The results of Y1 (entrapment efficiency), Y2 (size), and Y3 (drug release) are represented in Table 2. The preparation of gallic acid-loaded PLGA nanoparticles was performed using a single-step emulsification methodvi
dc.description.urihttps://link.springer.com/article/10.1186/s42269-022-00909-7vi
dc.languageen_USvi
dc.relation.ispartofseriesBulletin of the National Research Centre, Volume 46 (2022), Article number: 234vi
dc.subjectGallic acid/PLGA nanoparticlevi
dc.subjectFolate-tagged lipid nanoparticlesvi
dc.subjectPEGylationvi
dc.subjectCytotoxicityvi
dc.subjectCellular uptake studyvi
dc.subjectBreast cancer cellsvi
dc.titleEnhancing cellular uptake and membrane permeability of gallic acid for breast cancer therapy via folate-tagged PEGylated iron oxide nanoparticles has theronastic agentvi
dc.typeBBvi
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