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Effects of polymer degradation on drug release from PLGA‐mPEG microparticles: A dynamic study of microparticle morphological and physicochemical properties

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1097-4628(20001003)78:1<140::aid-app180>3.0.co;2-popenalex-snapshot
In vitro degradation and release profiles of poly-DL-lactide-poly(ethylene glycol) microspheres with entrapped proteins
inferredcites →https://doi.org/10.1002/adma.200390017openalex-snapshot
Uniform Emulsion‐Templated Silica Beads with High Pore Volume and Hierarchical Porosity
inferredcites →https://doi.org/10.1002/app.1990.070390101openalex-snapshot
Preparation, characterization, and properties of polylactide (PLA)–poly(ethylene glycol) (PEG) copolymers: A potential drug carrier
inferredcites →https://doi.org/10.1002/jps.20031openalex-snapshot
Methotrexate loaded poly(l-lactic acid) microspheres for intra-articular delivery of methotrexate to the joint
inferredcites →https://doi.org/10.1007/s11095-005-9042-6openalex-snapshot
Effect of Polymer Blending on the Release of Ganciclovir from PLGA Microspheres
inferredcites →https://doi.org/10.1016/0032-3861(88)90116-4openalex-snapshot
Thermal characterization of polylactides
inferredcites →https://doi.org/10.1016/0142-9612(95)93575-xopenalex-snapshot
Degradation of poly(lactic-co-glycolic acid) microspheres: effect of copolymer composition
inferredcites →https://doi.org/10.1016/0378-5173(86)90106-7openalex-snapshot
A physicochemical study of the morphology of progesterone-loaded poly (d,l-lactide) microspheres
inferredcites →https://doi.org/10.1016/0378-5173(95)04119-2openalex-snapshot
Effects of polymer degradation on drug released — mechanistic study of morphology and transport properties in 50:50 poly(dl-lactide-co-glycolide)
inferredcites →https://doi.org/10.1016/0378-5173(95)04258-xopenalex-snapshot
In vitro degradation of nanospheres from poly(D,L-lactides) of different molecular weights and polydispersities
inferredcites →https://doi.org/10.1016/j.addr.2004.09.003openalex-snapshot
Biodegradable poly(lactic-co-glycolic acid) microparticles for injectable delivery of vaccine antigens
inferredcites →https://doi.org/10.1016/j.conrel.2004.01.011openalex-snapshot
Effect of the size of biodegradable microparticles on drug release: experiment and theory
inferredcites →https://doi.org/10.1016/j.ijpharm.2004.11.017openalex-snapshot
Biodisposition of PEG-coated lipid microspheres of indomethacin in arthritic rats
inferredcites →https://doi.org/10.1016/j.ijpharm.2005.07.031openalex-snapshot
How porosity and size affect the drug release mechanisms from PLGA-based microparticles
inferredcites →https://doi.org/10.1016/j.jconrel.2004.01.011openalex-snapshot
Effect of the size of biodegradable microparticles on drug release: experiment and theory
inferredcites →https://doi.org/10.1016/j.jconrel.2004.07.029openalex-snapshot
Mapping neutral microclimate pH in PLGA microspheres
inferredcites →https://doi.org/10.1016/j.jconrel.2004.11.012openalex-snapshot
Modeling small-molecule release from PLG microspheres: effects of polymer degradation and nonuniform drug distribution
inferredcites →https://doi.org/10.1016/j.jconrel.2005.02.017openalex-snapshot
Effect of porosity on the release kinetics of propafenone-loaded PEG-g-PLA nanoparticles
inferredcites →https://doi.org/10.1016/s0142-9612(03)00419-8openalex-snapshot
Preparation and characterization of poly(lactic acid)–poly(ethylene glycol)–poly(lactic acid) (PLA–PEG–PLA) microspheres for controlled release of paclitaxel
inferredcites →https://doi.org/10.1016/s0142-9612(97)00098-7openalex-snapshot
Erosion of biodegradable block copolymers made of poly(d,l-lactic acid) and poly(ethylene glycol)
inferredcites →https://doi.org/10.1016/s0168-3659(01)00289-9openalex-snapshot
Fabrication of PLG microspheres with precisely controlled and monodisperse size distributions
inferredcites →https://doi.org/10.1016/s0168-3659(01)00530-2openalex-snapshot
PLGA–mPEG nanoparticles of cisplatin: in vitro nanoparticle degradation, in vitro drug release and in vivo drug residence in blood properties
inferredcites →https://doi.org/10.1016/s0168-3659(02)00136-0openalex-snapshot
Precise control of PLG microsphere size provides enhanced control of drug release rate
inferredcites →https://doi.org/10.1016/s0168-3659(02)00292-4openalex-snapshot
Effects of material hydrophobicity on physical properties of polymeric microspheres formed by double emulsion process
inferredcites →https://doi.org/10.1016/s0168-3659(03)00201-3openalex-snapshot
Polymer vesicles in vivo: correlations with PEG molecular weight
inferredcites →https://doi.org/10.1016/s0168-3659(98)00068-6openalex-snapshot
In vitro degradation study of polyester microspheres by a new HPLC method for monomer release determination
inferredcites →https://doi.org/10.1016/s0378-5173(97)00154-3openalex-snapshot
Drug release from PLA/PEG microparticulates
inferredcites →https://doi.org/10.1016/s0378-5173(98)00379-2openalex-snapshot
Investigation on process parameters involved in preparation of poly-?-lactide-poly(ethylene glycol) microspheres containing Leptospira Interrogans antigens
inferredcites →https://doi.org/10.1016/s0928-0987(02)00023-4openalex-snapshot
PLGA-based microparticles: elucidation of mechanisms and a new, simple mathematical model quantifying drug release
inferredcites →https://doi.org/10.1021/bm050228kopenalex-snapshot
How Autocatalysis Accelerates Drug Release from PLGA-Based Microparticles: A Quantitative Treatment
inferredcites →https://doi.org/10.1021/cm0492944openalex-snapshot
Synthesis of Hierarchically Porous Silica and Metal Oxide Beads Using Emulsion-Templated Polymer Scaffolds
inferredcites →https://doi.org/10.1021/ma00176a012openalex-snapshot
Poly(lactide-co-glycolide) decomposition kinetics in vivo and in vitro
inferredcites →https://doi.org/10.1023/a:1011043230573openalex-snapshot
In Vitro Protein Release and Degradation of Poly-dl-lactide-poly(ethylene glycol) Microspheres with Entrapped Human Serum Albumin: Quantitative Evaluation of the Factors Involved in Protein Release Phases
inferredcites →https://doi.org/10.1023/a:1024466407849openalex-snapshot
PLG Microsphere Size Controls Drug Release Rate Through Several Competing Factors

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4756000openalex-extracted
Prolonged Microcystis Restraint Through Allelochemicals Sustained-Release Microspheres Regulated by Carbon Material (Cm-Ac@Sm): Optimal Construction, Characterization, Effects and Synergistic Inhibition Mechanisms
inferred← citeshttps://doi.org/10.1002/adv.21887openalex-snapshot
The influence of hydrophilic mPEG segment on formation, morphology, and properties of PCL‐mPEG microspheres
inferred← citeshttps://doi.org/10.1002/app.41431openalex-snapshot
Effects of drug and polymer molecular weight on drug release from PLGA ‐m PEG microspheres
inferred← citeshttps://doi.org/10.1002/app.41943openalex-snapshot
Comparison of the degradation and release behaviors of poly(lactide‐co‐glycolide)–methoxypoly(ethylene glycol) microspheres prepared with single‐ and double‐emulsion evaporation methods
inferred← citeshttps://doi.org/10.1007/s10118-015-1660-9openalex-snapshot
A detailed view of PLGA-mPEG microsphere formation by double emulsion solvent evaporation method
inferred← citeshttps://doi.org/10.1007/s40199-019-00285-0openalex-snapshot
Probing the effect of various lipids and polymer blends on clopidogrel encapsulated floating microcarriers
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2013.07.056openalex-snapshot
Reduction-degradable PEG-b–PAA-b–PEG triblock copolymer micelles incorporated with MTX for cancer chemotherapy
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2021.111598openalex-snapshot
Microfluidic-assisted nanoprecipitation of biodegradable nanoparticles composed of PTMC/PCL (co)polymers, tannic acid and doxorubicin for cancer treatment
inferred← citeshttps://doi.org/10.1016/j.fjps.2016.08.001openalex-snapshot
Formulation of risperidone in floating microparticles to alleviate its extrapyramidal side effects
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.133661openalex-snapshot
Clinic-oriented injectable smart material for the treatment of diabetic wounds: Coordinating the release of GM-CSF and VEGF
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2010.07.052openalex-snapshot
Sustained prolonged topical delivery of bioactive human insulin for potential treatment of cutaneous wounds
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2013.11.058openalex-snapshot
Microparticles produced by the hydrogel template method for sustained drug delivery
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.175345openalex-snapshot
Prolonged Microcystis restraint through allelochemicals sustained-release microspheres regulated by carbon material (CM-AC@SM): Optimal formulation, characterization, effects and synergistic inhibition mechanisms
inferred← citeshttps://doi.org/10.1039/c5tb02468dopenalex-snapshot
Reverse micelles-in-microspheres with sustained release of water-soluble combretastatin A4 phosphate for S180 tumor treatment
inferred← citeshttps://doi.org/10.1208/s12249-023-02705-6openalex-snapshot
The Modified Exenatide Microspheres: PLGA-PEG-PLGA Gel and Zinc-Exenatide Complex Synergistically Reduce Burst Release and Shorten Platform Stage
inferred← citeshttps://doi.org/10.2174/1389201021666200101104116openalex-snapshot
Blending of PLGA-PEG-PLGA for Improving the Erosion and Drug Release Profile of PCL Microspheres
inferred← citeshttps://doi.org/10.3109/02652048.2014.995727openalex-snapshot
Drug-loaded PLGA-mPEG microparticles as treatment for atopic dermatitis-like skin lesions in BALB/c mice model
inferred← citeshttps://doi.org/10.3390/pharmaceutics18101239openalex-snapshot
Optimization of a Dexamethasone and Vitamin E PLGA Microparticle Formulation Intended for Posterior Segment of the Eye to Cope with Patients’ Anti-Inflammatory Needs
inferred← citeshttps://doi.org/10.4172/pharmaceutical-sciences.1000310openalex-snapshot
Preparation and In Vitro Evaluation of Biodegradable Microspheres with Narrow Size Distribution for Pulmonary Delivery
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