Physical-Chemical Characterization of Octreotide Encapsulated in Commercial Glucose-Star PLGA Microspheres.
Acylation
Drug Carriers
/ chemistry
Drug Compounding
/ methods
Drug Liberation
Drug Stability
Drugs, Generic
/ chemistry
Glucose
/ chemistry
Kinetics
Leuprolide
/ chemistry
Microspheres
Molecular Weight
Octreotide
/ chemistry
Polylactic Acid-Polyglycolic Acid Copolymer
/ chemistry
Porosity
Transition Temperature
PLGA
biodegradable microspheres
controlled-release
peptide delivery
peptide−polymer interactions
Journal
Molecular pharmaceutics
ISSN: 1543-8392
Titre abrégé: Mol Pharm
Pays: United States
ID NLM: 101197791
Informations de publication
Date de publication:
02 11 2020
02 11 2020
Historique:
pubmed:
3
9
2020
medline:
15
9
2021
entrez:
3
9
2020
Statut:
ppublish
Résumé
Sandostatin LAR (SLAR) is an injectable long-acting release (LAR) microsphere formulation for octreotide based on a biodegradeable glucose star copolymer of d,l-lactic and glycolic acids (PLGA-glu), which is primarily used for the treatment of patients with acromegaly. There currently is no generic SLAR approved in the United States despite expiration of patent coverage. To understand better this important formulation, SLAR was assessed for its composition and physical-chemical properties. Octreotide release kinetics was monitored under physiological conditions over 56 days together with several bioerosion parameters [mass loss, water uptake, pH of release media, polymer molecular weight (Mw), and confocal microscopy after BODIPY uptake]. A significant increase in the amount of released peptide occurred after day 14. After 1 day of incubation in PBST, octreotide was not extractable completely from SLAR during 2 h of the extraction process, but complete extraction was accomplished after 24 h, which suggested that strong and noncovalent PLGA-octreotide interactions occurred beginning in the initial release phase. Leuprolide is considered as a cationic peptide competitor for octreotide-PLGA interactions and its presence in the release medium resulted in more continuous octreotide release from SLAR, which was linearly correlated with the mass loss from the polymer (
Identifiants
pubmed: 32876463
doi: 10.1021/acs.molpharmaceut.0c00619
doi:
Substances chimiques
Drug Carriers
0
Drugs, Generic
0
Polylactic Acid-Polyglycolic Acid Copolymer
1SIA8062RS
Leuprolide
EFY6W0M8TG
Glucose
IY9XDZ35W2
Octreotide
RWM8CCW8GP
Types de publication
Journal Article
Research Support, U.S. Gov't, P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
4141-4151Subventions
Organisme : FDA HHS
ID : U01 FD005847
Pays : United States