Caffeine is a thermogenic agent that can be used in weight loss products. In order to achieve a sustained release of caffeine, silk fibroin (SF) film was uses as carrier. It has been shown that the loading method of caffeine into SF film affected the uniform distribution of caffeine in the SF film. When caffeine was added directly into SF solution, gelation has been occurred immediately and prevented the uniform distribution of caffeine. On the other hand, caffeine was dissolved in methanol in order to load the caffeine in SF film and crystallize the SF film at the same time. However, due to the fast evaporation of methanol, caffeine was recrystallized on the surface of SF film rather than penetrating into the film. Finally, caffeine was loaded into pre-crystallized SF film and uniform distribution of caffeine could be achieved. There was an initial burst of caffeine during the first 15 min, but after that a sustained release was achieved.
IntroductionObesity is one of the threats to the health of human and its control is important not only for personal health care but also for reducing social health care costs. The obesity is a result of excess energy intake over energy expenditure. Therefore, any substances which can increase the energy expenditure such as caffeine, ephedrine, capsaicin, and green tea can be used for obesity management (Diepvens et al., 2007). Caffeine is considered as a thermogenic agent, which inhibits the phosphodiesteraseinduced degradation of intracellular cyclic AMP (Dulloo, 1993).In the market, there are many weight loss products which contain caffeine as an active ingredient and various types of products are commercialized including ointments, creams and patches.Although caffeine is recognized as a safe material, overdose of caffeine can cause adverse effects such as palpitation, anxiety, headache, restlessness, and dizziness (Astrup et al., 1990). Therefore, in order to prevent the overdose of caffeine, a controlled release system is required.Silk fibroin (SF) has been used as a drug carrier for various drugs. The advantage of SF in drug delivery is that the entrapment of drug did not need any chemical cross-linking.SF became insoluble by various methods including exposure to alcohols or moisture. These methods promote the formation of β-sheet structure which acts as a physical cross-link, and thereby the activity loss of drug could be minimized.