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Magnetic Active Agent Release System (MAARS): Evaluation of a new way for a reproducible, externally controlled drug release into the small intestine

机译:磁性活性剂释放系统(MAARS):评估一种可重现的,外部控制的药物释放到小肠的新方法

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摘要

Human absorption studies are used to test new drug candidates for their bioavailability in different regions of the gastrointestinal tract. In order to replace invasive techniques (e.g. oral or rectal intubation) a variety of externally controlled capsule-based drug release systems has been developed. Most of these use ionizing radiation, internal batteries, heating elements or even chemicals for the localization and disintegration process of the capsule. This embodies potential harms for volunteers and patients. We report about a novel technique called Magnetic Active Agent Release System (MAARS), which uses purely magnetic effects for this purpose. In our trial thirteen healthy volunteers underwent a complete monitoring and release procedure of 250 mg acetylsalicylic acid (ASA) targeting the flexura duodenojejunalis and the mid-part of the jejunum. During all experiments MAARS initiated a sufficient drug release and was well tolerated. Beside this we also could show that the absorption of ASA is about two times faster in the more proximal region of the flexura duodenojejunalis with a tmax of 47 ± 13 min compared to the more distal jejunum with tmax values of 100 ± 10 min (p = 0.031).
机译:人体吸收研究用于测试候选新药在胃肠道不同区域的生物利用度。为了代替侵入性技术(例如口腔或直肠插管),已经开发了多种基于外部控制的基于胶囊的药物释放系统。这些中的大多数使用电离辐射,内部电池,加热元件甚至化学药品进行胶囊的定位和分解过程。这体现了对志愿者和患者的潜在危害。我们报告了一种称为磁性活性剂释放系统(MAARS)的新技术,该技术为此目的使用了纯磁性作用。在我们的试验中,十三名健康志愿者接受了针对硬膜十二指肠空肠和空肠中段的250 mg乙酰水杨酸(ASA)的完整监测和释放程序。在所有实验中,MAARS启动了足够的药物释放并且耐受性良好。除此之外,我们还可以表明,在十二指肠空肠近端区域中,ASA的吸收速度约为tmax值的最大值,即47±13分钟,而在远端空肠中,ASA的吸收速率约为100±10分钟(p = 0.031)。

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