The effect of a PEG versus a chitosan coating on the interaction of drug colloidal carriers with the ocular mucosa (Record no. 45202)

MARC details
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fixed length control field 02999nam a2200277Ia 4500
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control field MX-MdCICY
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250625140641.0
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-10974
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245 10 - TITLE STATEMENT
Title The effect of a PEG versus a chitosan coating on the interaction of drug colloidal carriers with the ocular mucosa
490 0# - SERIES STATEMENT
Volume/sequential designation European Journal of Pharmaceutical Sciences, 20(1), p.73-81, 2003
520 3# - SUMMARY, ETC.
Summary, etc. The influence of the surface characteristics of colloidal drug carriers in their interaction with different biological surfaces is becoming increasingly evident. In order to investigate the importance of these characteristics in their interaction with the ocular mucosa, we developed three types of nanocapsules that differ in their surface properties: poly-´-caprolactone (PECL)nanocapsules, chitosan (CS)-coated PECL nanocapsules and poly(ethylene glycol)(PEG)-coated PECL nanocapsules. Two different approaches were used to form these polymer coated nanocapsules: (i)the electrostatic anchorage of the coating onto the PECL nanocapsules-in the case of CS-and (ii)the use of the previously synthesized copolymer PECL-PEG for the formation of the nanocapsules. In both cases, the systems, prepared by the interfacial deposition technique, were loaded with a fluorescent dye (rhodamine)in order to quantify and visualize their interaction with the ocular surface ex vivo and in vivo. An important conclusion from the ex vivo studies is that the developed systems, and specially the CS-coated ones, enhanced the penetration of the encapsulated dye through the cornea. This effect was not simple due to the physical presence of the nanocapsules but to their ability to carry the encapsulated compound. The second conclusion from the confocal laser scanning microscopy (CLSM)studies is that the systems were able to enter the corneal epithelium by a transcellular pathway and that the penetration rate was dependent on the coating composition. The images suggest that the PEG coating accelerates the transport of the nanocapsules across the whole epithelium, whereas the CS coating favours the retention of the nanocapsules in the superficial layers of the epithelium. The specific behaviour of CS-coated systems was also corroborated in vivo. These results indicate that the surface composition of colloidal drug carriers affects their biodistribution in the eye. Therefore, this surface modification approach can be used as a targeting strategy in ocular drug delivery.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element OCULAR DRUG DELIVERY
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element NANOCAPSULES
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element CHITOSAN
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element POLYETHYLENE GLYCOL
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element CORNEAL TRANSPORT
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name De Campos, A.M.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Sánchez, A.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Gref, R.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Calvo, P.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Alonso, M.J.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/1I9hyK3XVWu3FkJ4qVfDHZp3u-pA_sqsH/view?usp=drivesdk">https://drive.google.com/file/d/1I9hyK3XVWu3FkJ4qVfDHZp3u-pA_sqsH/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-10974 25.06.2025 25.06.2025 Documentos solicitados