Bodor Miklós
University of Florida Gainesville, FL, Amerikai Egyesült Államok.
Bodor Laboratories, Inc. 4400 Biscayne Blvd., Suite 980, Miami, Florida 33137, Amerikai Egyesült Államok.
Orv Hetil. 2020 Mar;161(10):363-373. doi: 10.1556/650.2020.31657.
Retrometabolic drug design combines the structure-activity and structure-metabolism relationships, allowing the effective separation of drug action and side effects. This combination results in significant improvement of the therapeutic index. The main aim is not only to study the metabolism but to build into the drug molecule the desired metabolic route, in addition to the therapeutic activity. There are two basically different approaches to achieve this aim. Both use designed-in metabolism. The 1. chemical drug-targeting systems (CDS) and 2. soft drug, both control the drug targeting and action by strategically designed metabolism. In the case of the soft drugs, we want to rely on hydrolytic enzymes, avoiding the oxidative processes. In the present work, we focus on the clinical successes of the soft drugs designed in our laboratories. In order to show the difference, we briefly present a brain-targeted delivery system, where the originally inactive molecular construct undergoes sequential metabolism to allow specific concentration of the active drug in the brain. Among the soft drugs first we present the highly successful soft corticosteroids. Loteprednol etabonate has been used worldwide for over twenty years, and its use is constantly growing. In addition to the dramatically improved therapeutic index, the specific, serious ophthalmic side effects (elevation of intraocular pressure; glaucoma and cataract formation) were completely eliminated. Similarly designed second generation of soft corticosteroids are also presented, where the soft pharmacophore is structurally unexpected. The most recent soft drug design involves anticholinergics. Sofpironium bromide, a highly effective molecule but without the typical anticholinergic side effects, was first developed to treat hyperhidrosis, an unmet need. Phase III clinical studies were successfully completed and its marketing approval is pending. Since the soft drug design principles, methods and rules are general and specific in nature, a computerized expert system was also developed. Orv Hetil. 2020; 161(10): 363-373.
逆代谢药物设计结合了构效关系和构代关系,能有效分离药物作用和副作用。这种结合使治疗指数得到显著提高。其主要目的不仅是研究代谢,还要在药物分子中构建除治疗活性之外所需的代谢途径。有两种基本不同的方法来实现这一目标。两者都采用了设计好的代谢方式。1. 化学药物靶向系统(CDS)和2. 软药,二者都通过策略性设计的代谢来控制药物靶向和作用。对于软药,我们希望依靠水解酶,避免氧化过程。在本研究中,我们重点关注我们实验室设计的软药的临床成功案例。为了说明差异,我们简要介绍一种脑靶向递送系统,其中原本无活性的分子构建体经过一系列代谢,使活性药物在脑中达到特定浓度。在软药中,我们首先介绍非常成功的软皮质类固醇。氯替泼诺酯已在全球使用了二十多年,且其使用量在不断增加。除了显著提高的治疗指数外,特定的、严重的眼部副作用(眼压升高、青光眼和白内障形成)已完全消除。还介绍了类似设计的第二代软皮质类固醇,其软药效基团在结构上出人意料。最新的软药设计涉及抗胆碱能药物。溴化索非罗尼是一种高效分子,但没有典型抗胆碱能副作用,最初是为治疗多汗症这一未满足的需求而开发的。III期临床研究已成功完成,其上市批准正在等待中。由于软药的设计原则、方法和规则具有一般性和特殊性,还开发了一个计算机化专家系统。《匈牙利医学周报》。2020年;161(10): 363 - 373。