Nano/micro technologies for delivering macromolecular therapeutics using poly(D,L-lactide-co-glycolide)and its derivatives (Record no. 45178)

MARC details
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control field MX-MdCICY
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250625140641.0
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Transcribing agency CICY
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Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) B-10947
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245 10 - TITLE STATEMENT
Title Nano/micro technologies for delivering macromolecular therapeutics using poly(D,L-lactide-co-glycolide)and its derivatives
490 0# - SERIES STATEMENT
Volume/sequential designation Journal of Controlled Release, 125(3), p.193-209, 2007
520 3# - SUMMARY, ETC.
Summary, etc. Biodegradable nano/microparticles of poly(D,L-lactide-co-glycolide)(PLGA)and PLGA-based polymers are widely explored as carriers for controlled delivery of macromolecular therapeutics such as proteins, peptides, vaccines, genes, antigens, growth factors, etc. These devices are mainly produced by emulsion or double-emulsion technique followed by solvent evaporation or spray drying. Drug encapsulation, particle size, additives added during formulation, molecular weight, ratio of lactide to glycolide moieties in PLGA and surface morphology could influence the release characteristics. Encapsulation efficiency and release rates through nano/microparticle-mediated drug delivery devices can be optimized to improve their therapeutic efficacy. In this review, important findings of the past decade on the encapsulation and release profiles of macromolecular therapeutics from PLGA and PLGA-based nano/microparticles are discussed critically in relation to nature and type of bioactive molecule, carrier polymer and experimental variables that influence the delivery of macromolecular therapeutics. Even though extensive research on biodegradable microparticles containing macromolecular drugs has greatly advanced to the level of production know-how, the effects of critical parameters influencing drug encapsulation are not sufficiently investigated for nano-scaled carriers. The present review attempts to address some important data on nano/microparticle-based delivery systems of PLGA and PLGA-derived polymers with reference to macromolecular drugs.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PLGA
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element NANOPARTICLES
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Topical term or geographic name entry element MICROPARTICLES
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element TARGETED DRUG DELIVERY
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PROTEINS
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PEPTIDES
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Mundargi, R.C.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Babu, V.R.
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Personal name Rangaswamy, V.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Patel, P.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Aminabhavi, T.M.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/1ctUyyOn0aWYziXRr0lpMZ_v5cjKsOSB0/view?usp=drivesdk">https://drive.google.com/file/d/1ctUyyOn0aWYziXRr0lpMZ_v5cjKsOSB0/view?usp=drivesdk</a>
Public note Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx
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Source of classification or shelving scheme Clasificación local
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  Clasificación local     Ref1 CICY CICY Documento préstamo interbibliotecario 25.06.2025   B-10947 25.06.2025 25.06.2025 Documentos solicitados