2019
DOI: 10.1007/s11095-019-2640-5
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Proton Oriented-“Smart Depot” for Responsive Release of Ca2+ to Inhibit Peptide Acylation in PLGA Microspheres

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Cited by 6 publications
(2 citation statements)
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“…Even though PLA and PLGA nanoparticles showed good biocompatibility and bioavailability in a variety of drug delivery systems, two issues arise with their use. One is the stability of the loaded drug due to ionic interaction between the carboxy terminus of the biopolymer and the N-terminus of a protein-based drug [105,106]. The second is the formation of acidic residues (glycolic and lactic) in an aqueous environment, due to the erosion of the nanoparticle.…”
Section: Polylactic (Pla) Andmentioning
confidence: 99%
“…Even though PLA and PLGA nanoparticles showed good biocompatibility and bioavailability in a variety of drug delivery systems, two issues arise with their use. One is the stability of the loaded drug due to ionic interaction between the carboxy terminus of the biopolymer and the N-terminus of a protein-based drug [105,106]. The second is the formation of acidic residues (glycolic and lactic) in an aqueous environment, due to the erosion of the nanoparticle.…”
Section: Polylactic (Pla) Andmentioning
confidence: 99%
“…In addition to primary amines, arginine residue has also been identified as acylation site in goserelin and leuprolide having no primary amines [ 128 , 129 ]. Several strategies have been proposed and studied to prevent and minimize peptide acylation in PLGA formulations [ 134 , 135 , 136 , 137 , 138 , 139 , 140 , 141 , 142 , 143 , 144 , 145 ].…”
Section: Stability Of Drugs In Plga Particulate Formulationsmentioning
confidence: 99%