Posterior segment

后段
  • 文章类型: Journal Article
    扫频源光学相干断层扫描(SS-OCT)和扫频源光学相干断层扫描血管造影(SS-OCTA)的快速发展使眼睛的前后成像成为可能。这些技术已经从研究工具发展成为基本的临床成像模式。
    SS-OCT和SS-OCTA的波长较长,速度较快,有利于色素沉着组织下的结构和脉管系统的可视化,后段的视野更大,前段的可视化360度。在过去的10年里,处理OCT和OCTA数据的算法也极大地改善了图像质量,并实现了OCT和OCTA衍生指标的自动量化.这项技术丰富了我们目前对健康和患病眼睛的理解。尽管系统的高成本目前限制了SS-OCT和SS-OCTA在一开始的广泛使用,在过去的几年中,研究与临床实践之间的差距明显缩短。
    SS-OCT和SS-OCTA将继续快速发展,有助于在临床实践中更广泛采用新成像技术的范式转变。
    UNASSIGNED: The fast development of swept-source optical coherence tomography (SS-OCT) and swept-source optical coherence tomography angiography (SS-OCTA) enables both anterior and posterior imaging of the eye. These techniques have evolved from a research tool to an essential clinical imaging modality.
    UNASSIGNED: The longer wavelength and faster speed of SS-OCT and SS-OCTA facilitate better visualization of structure and vasculature below pigmented tissue with a larger field of view of the posterior segment and 360-degree visualization of the anterior segment. In the past 10 years, algorithms dealing with OCT and OCTA data also vastly improved the image quality and enabled the automated quantification of OCT- and OCTA-derived metrics. This technology has enriched our current understanding of healthy and diseased eyes. Even though the high cost of the systems currently limited the widespread use of SS-OCT and SS-OCTA at the first beginning, the gap between research and clinic practice got obviously shortened in the past few years.
    UNASSIGNED: SS-OCT and SS-OCTA will continue to evolve rapidly, contributing to a paradigm shift toward more widespread adoption of new imaging technology in clinical practice.
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  • 文章类型: Journal Article
    如何提高药物的生物利用度和延长药物在眼内的停留时间是传统眼给药的主要障碍。纳米技术因其具有减少不良反应的优点而被广泛应用于眼部给药系统,减少给药频率,延长释放时间,并提高药物在眼睛中的生物利用度。作为基于天然产品的纳米结构系统,生物启发的纳米结构系统具有较低的毒性,容易准备,成本效益高,在纳米技术领域具有潜在的应用价值。本文介绍了基于灵感来源和配方的生物启发纳米结构系统的系统分类及其在疾病中的简要应用。然后详细介绍了生物启发纳米结构系统用于治疗眼部疾病前后段的最新研究进展。最后,提供了当前的挑战和未来的方向,关于制造生物启发的纳米材料。
    How to enhance the bioavailability and prolong the residence time of drugs in the eye present the major barriers to traditional eye delivery. Nanotechnology has been widely used in ocular drug delivery systems because of its advantages of minimizing adverse reactions, decreasing the frequency of administration, prolonging the release time, and improving the bioavailability of the drug in the eye. As natural product-based nanostructured systems, bioinspired nanostructured systems have presented as less toxic, easy to prepare, and cost-effective and have potential application value in the field of nanotechnology. A systematic classification of bioinspired nanostructured systems based on their inspiration source and formulation and their brief applications in disease are presented here. A review of recent research progress of the bioinspired nanostructured systems for the treatment of the anterior and posterior segment of ocular disorders is then presented in detail. Finally, current challenges and future directions with regard to manufacturing bioinspired nanomaterials are provided.
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  • 文章类型: Journal Article
    眼药水是最常见和最方便的局部给药途径,也是许多眼部疾病的首选治疗方法。然而,传统滴眼液的眼部生物利用度(即,解决方案,悬架,和软膏)由于眼科生理和障碍而非常低,这极大地限制了他们的治疗效果。在过去的几十年里,许多新颖的滴眼剂给药系统,如前药,环糊精,原位凝胶,和纳米粒子,已被开发用于改善眼科生物利用度。这些新型滴眼剂给药系统具有良好的生物相容性,附着力,和性能,并显示出优于传统滴眼液的性能和功效。因此,本文综述了新型滴眼剂给药系统的研究进展,为剂型的开发提供参考,临床应用,和眼药水的商业转化。
    Eye drops are the most common and convenient route of topical administration and the first choice of treatment for many ocular diseases. However, the ocular bioavailability of traditional eye drops (i.e., solutions, suspensions, and ointments) is very low because of ophthalmic physiology and barriers, which greatly limits their therapeutic effect. Over the past few decades, many novel eye drop delivery systems, such as prodrugs, cyclodextrins, in situ gels, and nanoparticles, have been developed to improve ophthalmic bioavailability. These novel eye drop delivery systems have good biocompatibility, adhesion, and propermeation properties and have shown superior performance and efficacy over traditional eye drops. Therefore, the purpose of this review was to systematically present the research progress on novel eye drop delivery systems and provide a reference for the development of dosage form, clinical application, and commercial transformation of eye drops.
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  • 文章类型: Journal Article
    BACKGROUND: Posterior segment metallic intraocular foreign bodies (IOFBs) are a leading cause of visual morbidity and blindness, especially among young and middle-aged working populations. Here, we aimed to evaluate the surgical outcomes of the removal of such IOFBs that result from injuries.
    METHODS: In this retrospective study, 39 patients injured by metallic posterior segment IOFBs and who underwent primary repair procedures, vitrectomies, and IOFBs removal with or without procedures for traumatic cataract removal, scleral buckling and intraoperative tamponade application from January, 2008 to January, 2019. We analyzed the preoperative, intraoperative and postoperative related factors that affect the final visual outcomes.
    RESULTS: The mean age of the 39 patients was 40.51 ± 12.48 years with the male being predominent (100%).The mean preoperative vision measured 1.50 [Snellen Equivalent (SE), 20/645] ± 1.12 logMAR with the mean final vision measuring 0.93 (SE, 20/172) ± 1.09 logMAR. The related factors that were determined to affect the final visual outcomes included preoperative vision (P = 0.025), IOFB-related macula injuries (P = 0.001) and the development of postoperative complications (P = 0.005) especially retinal detachment (P = 0.002) with the mean final vision measuring 2.12 (SE, counting finger to hand motion) ±1.23 logMAR. Concerning the preoperative signs, the patients with preoperative endophthalmitis also obtained poor mean final vision measuring 1.30 (SE,20/400) ± 1.40 logMAR.
    CONCLUSIONS: IOFB-related macula injuries and postoperative retinal detachment were important related factors of poor final visual prognoses in cases involving posterior segment metallic IOFBs. Removing IOFB as early as possible may prevent preoperative endophthalmitis which could lead poor final visions even without significance.
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  • 文章类型: Journal Article
    作为视网膜视力受损的主要原因,黄斑水肿(ME)具有最高的临床治疗需求之一。目前对ME的治疗严重依赖侵入性技术,导致并发症和患者依从性差。为了提高曲安奈德作为眼后段滴眼液的效率,我们开发并表征了一种新的配方,即,曲安奈德壳聚糖涂层脂质体(TA-CHL),通过乙酸钙梯度法制备,并进行了一些修改。TA-CHL的平均粒径为135.46±4.49nm,包封效率高(90.66±3.21%),表现出持续释放的特征,优异的物理稳定性,对角膜没有明显的毒性,结膜,和视网膜.光学相干层析成像系统(OCT)用于检测体内CHL的药代动力学,表明CHL具有良好的药物递送效力。细胞摄取实验表明,CHL比脂质体具有更高的HCEC和ARPE-19转导效率。TA-CHL被证明是有助于眼睛后段的潜在有效滴眼剂。
    As a leading cause of vision impairment of the retina, macular edema (ME) has one of the highest clinical demands for treatment. Current treatment of ME relies heavily on invasive techniques resulting in complications and poor patient compliance. To enhance the efficiency of triamcinolone acetonide as eye drop to the posterior segment of the eye, we developed and characterized a novel formulation, namely, triamcinolone acetonide chitosan-coated liposomes (TA-CHL), prepared by the calcium acetate gradient method with some modifications. TA-CHL provided the mean particle size of 135.46 ± 4.49 nm and high entrapment efficiency (90.66 ± 3.21%), exhibited a sustained release profile, excellent physical stability, and no significant toxicity on cornea, conjunctiva, and retina. Optical coherence tomography system (OCT) was used to detect pharmacokinetics of CHL in vivo, indicating that CHL had good potency for drug delivery. Cellular uptake experiments showed CHL had the higher transduction efficiency into HCEC and ARPE-19 than liposomes. TA-CHL was shown to be potentially effective eye drop to contribute to the posterior segment of the eye.
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  • 文章类型: Journal Article
    To develop a standardised grading scheme, using standard photos, for spectral-domain ocular coherence tomography (SD-OCT) images of the posterior eye and evaluate the interobserver agreement among trained ophthalmologists in identifying pathological changes.
    Subjects were recruited from Liwan District, Guangzhou, with SD-OCT data collection from June 2013 to November 2013 as part of 10-year follow-up visits from the Liwan Eye Study. All subjects underwent SD-OCT imaging of the macula with scanning lines analysed by two ophthalmologists to assess for the presence of 12 different posterior segment lesions. Per cent agreement for each lesion between the graders and quantitative measures of dome-shaped macula (DSM) height and choroidal thickness were calculated.
    A total of 679 SD-OCT images from 679 subjects were independently evaluated by the two graders. Each of the 12 lesions was successfully graded as present or absent in over 96% of images. For all lesions, per cent agreement between observers was over 90%, ranging from 90.7% for epiretinal membranes and retinal pigment epithelium thickenings to 99.7% for full thickness macular holes and retinal detachments. Quantitative measurements of DSM height and choroidal thickness at three locations of the eye all exhibited intraclass correlation scores between the two graders of greater than 0.9.
    Our study demonstrates high concordance between graders in characterising posterior segment lesions using SD-OCT images, validating the continued use of this imaging modality in the diagnosis of posterior eye disease.
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  • 文章类型: Journal Article
    目的是研究阿昔洛韦生物不稳定氨基酸酯前药(ACV-X,X=Arg,Gly和Trp)作为增加ACV的眼部生物利用度的手段。前药表现出对水解的组织依赖性敏感性。ACV-Arg离子电渗疗法,ACV-Gly和ACV-Trp(5mM,0.5mA/cm2)持续5分钟,然后进行55分钟的被动扩散导致明显的角膜沉积(分别为21.5±5.1、14.1±2.0和5.3±0.6nmol/cm2)和角膜渗透(分别为13.9±1.6、10.9±1.8和5.7±0.5nmol/cm2)。相比之下,1小时后通过猪角膜被动递送ACV The objective was to investigate (trans)corneal and transscleral iontophoresis of biolabile amino acid ester prodrugs of aciclovir (ACV-X, X = Arg, Gly and Trp) as a means to increase ocular bioavailability of ACV. Prodrugs displayed tissue-dependent susceptibility to hydrolysis. Iontophoresis of ACV-Arg, ACV-Gly and ACV-Trp (5 mM, 0.5 mA/cm2) for 5 min followed by 55 min passive diffusion resulted in appreciable corneal deposition (21.5 ± 5.1, 14.1 ± 2.0 and 5.3 ± 0.6 nmol/cm2, respectively) and transcorneal permeation (13.9 ± 1.6, 10.9 ± 1.8 and 5.7 ± 0.5 nmol/cm2, respectively) of ACV species. In contrast, passive delivery of ACV across porcine cornea after 1 h was < LOQ (i.e. <0.125 nmol/cm2). Transscleral permeation of ACV-Arg, ACV-Gly and ACV-Trp (9 mM, 1.25 mA/cm2) after iontophoresis for 5 min was 20.4 ± 3.8, 12.3 ± 0.3 and 8.4 ± 0.4 nmol/cm2, respectively - far superior to passive delivery which was again < LOQ. Using intact porcine eye globes, 5 min transscleral iontophoresis of ACV-Gly at 3.75 mA/cm2 resulted in considerable delivery of ACV species to the choroid/retina and vitreous humour (5.7 ± 2.3 and 11.7 ± 3.7 nmol/cm2, respectively). Furthermore, the average concentration of ACV species in the whole eyeball (4.5 ± 1.6 nmol/cm3) was significantly higher than the IC50 of ACV against HSV-1 (<0.22 nmol/cm3), demonstrating the potential application for the treatment of ocular HSV infections.
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  • 文章类型: Journal Article
    皮质类固醇已用于治疗眼后段疾病,但是将药物输送到后段仍然是一个需要解决的问题。在我们的研究中,我们探讨了Sub-tenon的可控连续药物递送到眼后段的可行性。可控制的连续亚腱给药(CCSDD)系统,静脉注射(IV)和结膜下注射(SC)用于在兔体内递送地塞米松磷酸二钠(DEXP),在首次注射后24h,通过ShimadzuLC-MS2010系统在不同时间点测量眼部后段组织中的地塞米松浓度.在CCSDD中,12、24小时的地塞米松水平明显高于其他两种方法,CCSDD在3、6h时比玻璃体中的IV时高(p<0.01);CCSDD在6、12、24h时比其他两种方法高,CCSDD中的1、3h比视网膜/脉络膜复合物中的IV高(p<0.01);CCSDD中的3、6、12、24h比其他两种方法高,CCSDD在1h时比巩膜IV时高(p<0.05)。在所有眼后段组织中,CCSDD组中的AUC0-24高于其他两组。我们的结果表明,地塞米松浓度可以在后段通过CCSDD比SC和IV维持适度高,表明CCSDD可能是治疗各种难治性后段疾病的替代治疗方法。
    Corticosteroids have been used for treatment of posterior segment eye diseases, but the delivery of drug to the posterior segments is still a problem to resolve. In our study, we explore the feasibility of Sub-tenon\'s Controllable Continuous Drug Delivery to ocular posterior segment. Controllable continuous sub-tenon drug delivery (CCSDD) system, intravenous injections (IV) and sub-conjunctival injections (SC) were used to deliver dexamethasone disodium phosphate (DEXP) in rabbits, the dexamethasone concentration was measured in the ocular posterior segment tissue by Shimadzu LC-MS 2010 system at different time points in 24 h after first dose injection. Levels of dexamethasone were significantly higher at 12, 24 h in CCSDD than two other approaches, and at 3, 6 h in CCSDD than IV in vitreous body (p < 0.01); at 6, 12, 24 h in CCSDD than two other approaches, and at 1, 3 h in CCSDD than IV in retinal/choroidal compound (p < 0.01); at 3, 6, 12, 24 h in CCSDD than two other approaches, and at 1 h in CCSDD than IV in sclera (p < 0.05). The AUC0-24 in CCSDD group is higher than two other groups in all ocular posterior segment tissue. Our results demonstrated that dexamethasone concentration could be sustained moderately higher in the posterior segment by CCSDD than SC and IV, indicating that CCSDD might be a therapeutic alternative to treat a variety of intractable posterior segment diseases.
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