2021
DOI: 10.1016/j.ijpharm.2021.120807
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PLGA-based nanomedicines manufacturing: Technologies overview and challenges in industrial scale-up

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Cited by 138 publications
(99 citation statements)
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“…It is currently undergoing Phase III clinical trials for access to the EU and US markets. For the NPs, only one Phase II clinical trial based on PEG-PLGA/PLA-PEG NPs (BIND-014) for metastatic castration-resistant prostate cancer was reported [ 15 ]. However, in the case of NDDs treatment, no PLGA NPs are currently on the market or in clinical trials, but are currently only at the preclinical stage [ 16 ].…”
Section: Plga Npsmentioning
confidence: 99%
“…It is currently undergoing Phase III clinical trials for access to the EU and US markets. For the NPs, only one Phase II clinical trial based on PEG-PLGA/PLA-PEG NPs (BIND-014) for metastatic castration-resistant prostate cancer was reported [ 15 ]. However, in the case of NDDs treatment, no PLGA NPs are currently on the market or in clinical trials, but are currently only at the preclinical stage [ 16 ].…”
Section: Plga Npsmentioning
confidence: 99%
“…PLGA micro/nanoparticle have a variety of morphological structures, including solid, porous, core-shell structure and multi-compartment particles. Porous particles and core-shell particles are the most widely used types at present, and they can realize the co-delivery of multiple drugs [11,58]. Single-layer polymer carriers prepared based on PLGA are widely used to deliver hydrophilic or hydrophobic drugs [59].…”
Section: Types Of Plga Micro/nanoparticlementioning
confidence: 99%
“…Developing an efficient drug delivery system for cancer has become a research hotspot in the biomedical field [11]. Researchers have prepared various micro/nanoparticle as delivery vehicle [12], breaking through the restriction of free drug applications [13].…”
Section: Introductionmentioning
confidence: 99%
“…Good manufacturing practices verification is required to ensure conformance in large-scale production [ 6 ]. In addition, to evaluate whether DDS large-scale production influences clinical performance, comprehensive quality controls of drug carriers are essential [ 8 ]. Finally, clinical trials are mandatory to determine the ratio between benefits and risks of the developed DDS [ 6 ].…”
Section: Introductionmentioning
confidence: 99%