4.4 Article

A Preservative-and-Fluorescein Interaction Model for Benign Multipurpose Solution-Associated Transient Corneal Hyperfluorescence

期刊

CORNEA
卷 31, 期 12, 页码 1480-1488

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/ICO.0b013e31824a2083

关键词

fluorescein; multipurpose solution; hyperfluorescence; staining

资金

  1. Bausch Lomb

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Purpose: Multipurpose contact lens solution (MPS)/preservative-associated transient corneal hyperfluorescence has been suggested to represent corneal injury. To determine the validity of this assumption, the molecular-level interactions of common disinfectants in soft contact lens MPS and the corneal epithelium using an in vitro model were assessed. Methods: A liposome-based model of the corneal epithelial surface was developed and used to assess the interactions of polyhexamethylene biguanide (PHMB), polyquaternium-1 (PQ-1), and fluorescein with membrane components and the effects of PHMB and PQ-1 on membrane integrity. The fluorescence anisotropy (a measure of interactions between molecules) was determined. Liposome integrity was assessed by measuring the liposome melting point temperature. Results: Free fluorescein did not associate with the liposome (P > 0.4). Both fluorescein-tagged PHMB and PQ-1 associated with liposomes (P < 0.002 and P <= 0.01, respectively); however, only PHMB induced free fluorescein association with membrane components. At physiological temperature, no significant shift in the melting point temperature was observed when liposomes were exposed to PHMB from 0 to 100 ppm (P > 0.05). In contrast, exposure of >7 ppm PQ-1 disrupted the liposomes. Conclusions: Based on this study, PHMB-to-liposome bilayer interaction is nondestructive, even at concentrations 100 times higher than found in commercially available MPS products. In contrast, PQ-1-to-liposome bilayer interaction led to liposome disruption. This study presents molecular-level evidence to support that preservative-associated transient corneal hyperfluorescence is a benign transient phenomenon and its evaluation clinically may be an ambiguous strategy for determining biocompatibility and cell surface integrity.

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