2012
DOI: 10.1016/j.biomaterials.2012.03.056
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Multidrug release based on microneedle arrays filled with pH-responsive PLGA hollow microspheres

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Cited by 128 publications
(76 citation statements)
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“…We chose these needle sizes because the usefulness of these microneedles are commonly investigated. 17,19,37) Microneedles having a needle length of 500 µm were likely to be more effective than 300-µm microneedles in terms of activation of MHC class II on LCs (Fig. 5).…”
Section: Discussionmentioning
confidence: 99%
“…We chose these needle sizes because the usefulness of these microneedles are commonly investigated. 17,19,37) Microneedles having a needle length of 500 µm were likely to be more effective than 300-µm microneedles in terms of activation of MHC class II on LCs (Fig. 5).…”
Section: Discussionmentioning
confidence: 99%
“…The obtained IONPs were then thoroughly rinsed by acetone to remove the free oleic acid. HMs of PLGA (10 mg/mL) that contained IONPs (6 mg/mL) and DOX (1 mg/mL) were prepared using a water-in-oil-in-water (W/O/W) double-emulsion, solvent-diffusion-evaporation technique, which has been described previously [19,20]. The T g of PLGA HMs was evaluated using a differential scanning calorimeter (DSC, PerkinElmer, Norwalk, CT, USA); the heating rate was controlled at 10 C/min, and each sample was heated and cooled for five cycles between 20 and 60 C.…”
Section: Preparation and Characterization Of Lipos-hmsmentioning
confidence: 99%
“…The excipient of maltose in SH-DM dissolved quickly after tissue fluid absorption and drug started to release. The degradation of PLGA was slow 61 , which acted as the skeleton of DM and postponed microchannels closing. This design further enhanced the drug permeability into skin.…”
Section: Pharmacokineticsmentioning
confidence: 99%