首页> 外文期刊>Drugs in R&D >Analysis of Lipid Peroxidation and Electron Microscopic Survey of Maturation Stages during Human Cataractogenesis Pharmacokinetic Assay of Can-C~(TM) N-Acetylcarnosine Prodrug Lubricant Eye Drops for Cataract Prevention
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Analysis of Lipid Peroxidation and Electron Microscopic Survey of Maturation Stages during Human Cataractogenesis Pharmacokinetic Assay of Can-C~(TM) N-Acetylcarnosine Prodrug Lubricant Eye Drops for Cataract Prevention

机译:Can-C〜(TM)N-乙酰基肌肽前药润滑剂滴眼液在人白内障发生过程中脂质过氧化的分析和成熟阶段的电子显微镜观察,以预防白内障

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Morphological and biophysical techniques described in this study have shown that membrane derangement occurs in human cataractous lenses.The data suggest that these disruptions were globules,vacuoles,multilamellar membranes and clusters of highly undulating membranes.Deleterious structural damage of the lens fibre cell plasma membranes serve as the primary light-scattering centres that cause the observed lens opacity.Nuclear cataract,a major cause of loss of lens transparency in the aging human,has been thought to be associated with oxidative damage,particularly at the site of the nuclear plasma membrane.Phospholipid molecules modified by oxygen accumulate in the lipid bilayer,change its geometry and impair lipid-lipid and protein-lipid interactions in lenticular fibre membranes.lipid peroxidation(LPO)is a causative and pathogenic factor in cataract.Increased concentrations of primary molecular LPO products(diene conjugates,lipid hydroperoxides,oxy-derivatives of phospholipid fatty acids)and end-fluorescent LPO products have been detected in the lipid moieties of aqueous humour samples and human lenses obtained from patients with senile and complicated cataracts as compared with normal donors.In the present study,a rapid and simple high-performance liquid chromato-graphic(HPLC)assay for determination of imidazole-containing dipeptides in the aqueous humour of the eye was developed.The method was applied to determine the pharmacokinetic parameters and the time-course of N-acetylcarnosine and L-carnosine-related product in the eye,following a single dosage of topical ocular administration of peptide.Utilising data from pharmacokinetic studies and the specific purity of the N-acetylcarnosine(NAC)ingredient as a source of the pharmacological principle L-carnosine,we have created an ophthalmic time-release prodrug form including the US FDA-approved carboxymethylcellulose lubricant and other essential ingredients(Can-C~(TM),private label Nu-Eyes~(TM)).This formulation increases the intraocular absorption of L-carnosine in the aqueous humour and optimises its specific antioxidant activity in vivo while reducing the toxic effects of lipid peroxides on the crystalline lens.L-carnosine that enters the aqueous humour can accumulate in the lens tissue for a reasonable period of time.The presence of L-carnosine in transparent crystalline lenses during normal aging was detected and its concentration in this case was about 25muM.At different stages of cataract development,the level of L-carnosine drastically decreased,reaching about 5 mu M in ripe human cataracts.However,administration of pure L-carnosine(1% solution)to the rabbit eye(instillation or subconjunctival injection)does not lead to accumulation of this natural compound in the aqueous humour at the time level over 30 minutes at a concentration exceeding that in placebo-treated matched eyes,and its effective concentration is exhausted more rapidly.Use of NAC prodrug eye drops optimises the clinical effects of L-carnosine in the treatment of ophthalmic disorders(such as prevention and reversal of cataracts in human and animal [canine] eyes).The data provided predict a clinical effect with NAC ophthalmic prodrug,and show that the magnitude and duration of this effect are directly related to the bioavailability of L-carnosine released from NAC in the aqueous humour of the anterior eye segment.The ophthalmic NAC drug shows promise in the treatment of a range of ophthalmic disorders that have a component of oxidative stress in their pathogenesis(including cataract,glaucoma,dry eye,vitreous floaters,inflammatory disorders,and corneal,retinal and systemic diseases [such as diabetes mellitus and its ophthalmic complications]).There is a need for further and better collaboration between Innovative Vision Products' cataract control and ophthalmic services,improved education of people affected by cataract,a commitment that N-acetylcarnosine eye drops will be the preferred treatment before orth
机译:这项研究描述的形态学和生物物理技术表明,人白内障晶状体会发生膜排列紊乱。数据表明,这些破坏是小球,空泡,多层膜和高度起伏的膜簇。晶状体纤维细胞质膜的结构性损伤受到损害。作为导致老年人晶状体不透明的主要光散射中心。核白内障是老年人衰老的晶状体透明性丧失的主要原因,据认为与氧化损伤有关,尤其是在核质膜部位。氧修饰的磷脂分子积聚在脂质双层中,改变其几何结构并损害双凸状纤维膜中的脂质-脂质和蛋白质-脂质相互作用。脂质过氧化(LPO)是白内障的致病性和致病因素。初级分子LPO产物浓度升高(二烯共轭物,脂质氢过氧化物,磷脂脂肪酸的氧衍生物与正常供体相比,在患有老年和复杂性白内障患者的房水样本和人晶状体的脂质部分中检测到了ds)和末端荧光LPO产物。在本研究中,本研究建立了一种快速简便的高效液相色谱仪建立了测定眼房水中含咪唑二肽的图形化(HPLC)测定方法,该方法用于测定眼内房水中N-乙酰肌氨酸和L-肌氨酸相关产物的药代动力学参数和时程。眼,单次局部肽给药。利用药代动力学研究的数据和N-乙酰肌肽(NAC)成分的特定纯度作为L-肌肽的药理学原理,我们开发了眼用缓释剂前药形式包括美国FDA批准的羧甲基纤维素润滑剂和其他必要成分(Can-C〜(TM),私有标签Nu-Eyes〜(TM))。减轻眼房水中L-肌肽的眼内吸收并优化其体内特定的抗氧化活性,同时减少脂质过氧化物对晶状体的毒性作用。进入房水的L-肌肽可以在晶状体组织中积累,从而达到合理的吸收效果。在正常老化过程中,检测到透明晶体镜片中存在L-肌氨酸,其浓度约为25μM。在白内障发展的不同阶段,L-肌氨酸的水平急剧下降,达到约5μM。然而,将纯天然左旋肌肽(1%溶液)给予兔眼(滴注或结膜下注射)并不会导致这种天然化合物在30分钟的时间水平内在房水中积聚。 NAC前药滴眼液的浓度超过了安慰剂治疗的配对眼中的浓度,并且有效浓度被更快地耗尽。使用NAC前药滴眼液可优化临床疗效-肌肽在眼科疾病治疗中的作用(例如预防和逆转人和动物[犬]眼的白内障)。提供的数据预测了NAC眼科前药的临床疗效,并显示了这种作用的程度和持续时间这种作用与从NAC释放的L-肌肽在眼前节房水中的生物利用度直接相关。眼科NAC药物在治疗一系列眼病中具有前景,这些眼病在其发病机理中具有氧化应激的成分(包括白内障,青光眼,干眼,玻璃体漂浮物,炎症性疾病以及角膜,视网膜和全身性疾病(例如糖尿病及其眼科并发症)。)Innovative Vision Products的白内障控制与眼科服务,改善对白内障患者的教育,承诺N-乙酰肌肽滴眼液将成为矫正前的首选治疗方法

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