Characterization of the degradation mechanisms of lysine-derived aliphatic poly (ester urethane)scaffolds (Record no. 48112)

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fixed length control field 02920nam a2200313Ia 4500
003 - CONTROL NUMBER IDENTIFIER
control field MX-MdCICY
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250625153931.0
040 ## - CATALOGING SOURCE
Transcribing agency CICY
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) B-13915
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245 10 - TITLE STATEMENT
Title Characterization of the degradation mechanisms of lysine-derived aliphatic poly (ester urethane)scaffolds
490 0# - SERIES STATEMENT
Volume/sequential designation BioMaterials, 32, p.419--29, 2011
520 3# - SUMMARY, ETC.
Summary, etc. Characterization of the degradation mechanism of polymeric scaffolds and delivery systems for regenerative medicine is essential to assess their clinical applicability. Key performance criteria include induction of a minimal, transient inflammatory response and controlled degradation to soluble noncytotoxic breakdown products that are cleared from the body by physiological processes. Scaffolds fabricated from biodegradable poly(ester urethane)s (PEURs)undergo controlled degradation to noncytotoxic breakdown products and support the ingrowth of new tissue in preclinical models of tissue regeneration. While previous studies have shown that PEUR scaffolds prepared from ysine-derived polyisocyanates degrade faster under in vivo compared to in vitro conditions, the degradation mechanism is not well understood. In this study, we have shown that PEUR scaffolds prepared from lysine triisocyanate (LTI)or a trimer of hexamethylene diisocyanate (HDIt)undergo hydrolytic, esterolytic, and oxidative degradation. Hydrolysis of ester bonds to yield a-hydroxy acids is the dominant mechanism in buffer, and esterolytic media modestly increase the degradation rate. While HDIt scaffolds show a modest (<20 percent)increase in degradation rate in oxidative medium, LTI scaffolds degrade six times faster in oxidative medium. Furthermore, the in vitro rate of degradation of LTI scaffolds in oxidative medium approximates the in vivo rate in rat excisional wounds, and histological sections show macrophages expressing myeloperoxidase at the material surface. While recent preclinical studies have underscored the potential of injectable PEUR scaffolds and delivery systems for tissue regeneration, this promising class of biomaterials has a limited regulatory history. Elucidation of the macrophage-mediated oxidative mechanism by which LTI scaffolds degrade in vivo provides key insights into the ultimate fate of these materials when injected into the body.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element POLYURETHANE
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element BIODEGRADATION
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element MACROPHAGE
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element OXIDATION
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element HYDROLYSIS
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element SCAFFOLD
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Hafeman, A.E.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Katarzyna, J.Z.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Zachman, A.L.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Hak-Joon, S.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Nanney, L.B.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Davidson, J.M.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Guelcher, S.A.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/165ussLROzZGI1JuM31wBO0FeZbHkV0es/view?usp=drivesdk">https://drive.google.com/file/d/165ussLROzZGI1JuM31wBO0FeZbHkV0es/view?usp=drivesdk</a>
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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-13915 25.06.2025 25.06.2025 Documentos solicitados