Wei He

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Name: 何伟
Organization: Shenyang Pharmaceutical University , China
Department: Department of Chemistry
Title: Professor(PhD)

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Co-reporter:Abir Bouledjouidja, Yasmine Masmoudi, Yanfeng Li, Wei He, Elisabeth Badens
Journal of Cataract & Refractive Surgery 2017 Volume 43, Issue 10(Volume 43, Issue 10) pp:
Publication Date(Web):1 October 2017
DOI:10.1016/j.jcrs.2017.07.033
PurposeTo prepare drug-loaded intraocular lenses (IOLs) used to combine cataract surgery with postoperative complication treatment through supercritical impregnation while preserving their optical properties.SettingAix-Marseille Université, CNRS, Centrale Marseille, Laboratoire de Mécanique, Modélisation & Procédés Propres, Marseille, France, and He University Eye Hospital, Liaoning Province, China.DesignExperimental study.MethodsSupercritical impregnations of commercial foldable IOLs used in cataract surgery with ciprofloxacin (an antibiotic) and dexamethasone 21-phosphate disodium salt (an antiinflammatory drug) were performed in a noncontinuous mode. Impregnation amounts were determined through drug-release kinetic studies. The optical characterizations of IOLs were determined by evaluating the dioptric power and the imaging quality by determining the modulating transfer function (MTF) at a specified spatial frequency according to the International Organization for Standardization (ISO 11979-2:2014).ResultsTransparent IOLs presenting an effective impregnation were obtained with a prolonged drug delivery during approximately 10 days. Optical characterizations (dioptric powers and MTF values) show preserved optical properties after supercritical treatment/impregnation.ConclusionSupercritical treatments/impregnations do not damage the optical properties of IOLs and are therefore adequate for the preparation of delivery devices used for cataract surgery.
Co-reporter:Mingqi Zhang, Fenglei Zhang, Jin Sun, Yan Sun, Ling Xu, Donglei Zhang, Zhuoshi Wang, Wei He
Neuroscience Letters 2017 Volume 657(Volume 657) pp:
Publication Date(Web):14 September 2017
DOI:10.1016/j.neulet.2017.07.053
•The condition medium of human mesenchymal stem cells can enhance the proliferation capacity of human retinal progenitor cells.•The condition medium of human mesenchymal stem cells can promote human retinal progenitor cells adherence.•The condition medium of human mesenchymal stem cells favours human retinal progenitor cells differentiation towards retinal neurons.Retinal progenitor cell is a promising candidate in the treatment of retinal pigmentosa diseases. The limiting factors of stem cell transplantation are the proliferation and differentiation capacities of hRPCs, which may be governed by culture conditions. Previous studies have proved that the secretome of human Umbilical Cord Mesenchymal stem cells (hUCMSCs) and human Adipose derived stem cells (hADSCs), including more active cytokines and neurotrophic factors, have the paracrine potential of enhancing proliferation and differentiation in several cell types. The aim of this study was to investigate whether hRPCs could effectively proliferate, adhere and differentiate towards specific retinal cell types by treating with the condition medium (CM) of hUCMSCs (hUCMSCCM) or hADSCs (hADSCCM). Here, we show that hUCMSCCM or hADSCCM enhances the proliferation rate of the S and G2 phase cells, with an upregulation of Ki67 expression. Moreover, the upregulation expression of NF, Recoverin and Rhodopsin indicates that specialized retinal cells including ganglion cells and photoreceptors are favored over hRPCs differentiation due to hUCMSCCM or hADSCCM. Under FBS induced differentiation conditions, hRPCs treated with hUCMSCCM or hADSCCM increase the expression of retinal neuron and photoreceptor specific markers. These results suggest that hUCMSCCM and hADSCCM can stimulate the hRPC proliferation, promote its adherence and support hRPC neuronal and photoreceptor differentiation. These findings may provide a new strategy to improve the viability of hRPCs and photoreceptor differentiation capacities.Download high-res image (133KB)Download full-size image
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