2 research outputs found

    Potential use of glucosamine, chondroitine, chitosan and phytoestrogen for patients with osteoarthritis

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    The burden of musculoskeletal disease has increased significantly to become the second leading cause of YLD (years of life with disability). Osteoarthritis (OA) therapy that is often given is ibuprofen (NSAID) often give side effects. Therefore, it is necessary to conduct a literature review to explore evidence of how much potential these materials have for treating OA. The literature review was conducted on four databases, e.g., Pubmed, Scopus, Science direct, Clinical Key. We used several keywords to find each topic of discussion. Topic 1, benefits of glucosamine chondroitine; topic 2, benefits of chitosan; topic 3, benefits of phytoestrogens. Data from included studies were then extracted. Obtained data were analyzed using descriptive statistical methods. Glucosamine-chondroitin had a significant effect in reducing pain, reducing inflammation, reducing the rate of joint space narrowing and helping to improve joint function in OA patients with long-term use. Furthermore, the potential of chitosan can help bone remodeling, reduce pain, and inflammation. Besides, phytoestrogens also have the potential to increase bone mineral density, reducing the rate of bone turnover and reduce the occurrence of obesity through its anti-cholesterol effects. The complexity of the mechanism of action given, ranging from preventing the biggest risk factor, namely obesity; treating the main causes such as inflammation and cartilage damage; and also to treating the symptoms such as joint pain and stiffness. In the future, it is necessary to conduct clinical trials study using the ingredients glucosamine, chondroitin, chitosan and phytoestrogens to treat patients with OA

    Bioassay Guided Fractionation of Ciplukan (Physalis angulata L.) monitored by Glucose Consumption Assay and Thin Layer Chromatography on Myoblast Cells

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    Ciplukan (Physalis angulata Linn.) has been used by the community as an anti-diabetic drug. The antidiabetic effect is due to ingredients such as unsaturated fatty acids, alkaloids, flavonoids, saponins, polyphenols, steroids, triterpenoids, monoterpenoids, and sesquiterpenoids. Part of the fruit of P. angulata contains many active substances of flavonoids with the proportion of fruit extract 300 μg/ml is 84%. Therefore the exploration for compounds responsible for antidiabetic activity in P. angulata needs to be done to ensure empirical evidence. The purpose of this study was to find the active fraction of P. angulata L. which has anti-hyperglycemic properties. This study used Myoblast cells as subjects and the Bioassay Guided Fractionation method for separating compound groups through three stages of the extraction, partitioning, and fractionation processes which were monitored using TLC and the Glucose Consumption Assay test. The results showed that the chloroform extract (CHCl3) was more active in lowering glucose levels compared to the methanol extract (MeOH) (4.86% vs -8.74%). MeOH insoluble extract was more active than MeOH soluble extract (5.14% vs -8.52). The fractionation results showed that Fraction I was the most active in lowering glucose levels compared to FII, III, and IV (26.47%; 13.18%; 0.15%; 13.76%). Therefore Fraction 1 which contains a class of flavonoid compounds is a potential candidate to be developed as an antidiabetic agent
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