Vitamin C Essay

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UV exposure to skin can generate reactive oxygen species (ROS) that cause direct chemical alteration in collagen and increase matrix metalloproteinase (MMP) production leading to collagen break down. In addition, ROS produce mediators that cause skin inflammation. Vitamin C neutralizes ROS and is equally effective against UVA (320-400nm) and UVB (290-320 nm) that are produced due to UV exposure and causes skin-aging and sunburns respectively. Vitamin C is most effective as it exerts its action interacellularly and extracellularly (7). A study carried out by Telang (2013)(14) showed that 10 % of vitamin C applied topically decrease UVB induced erythema by 52% and sunburn cell formation by 40-60%. Vitamin C has a role to reduce the melanin formation by inhibition of tyrosinase enzyme that decrease dark spots. It has photo aging protection due to promoting collagen synthesis, as it is essential cofactor for enzymes required for its biosynthesis as a result, decrease wrinkle appearance (15). Therefore, extensive research was carried on for the maximum protection of vitamin C maintaining the stability, pH sensitivity and permeation to the skin. Summary of Preferred Solution N-acyl chitosan nanoparticles loaded with vitamin C: Fig.4. Chitosan structure (16) In this case study, our concern goes for the chitosan nanoparticles; firstly nanoparticles are able to adsorb and/or encapsulate a drug, thus protecting it against chemical and enzymatic degradation. Furthermore the encapsulated drug may be prevented from crystallization, thus forming a solid solution. Depending on drug solubility in the carrier, a drug load varying from only a few percent up to 50%] Secondly, chitosan is ... ... middle of paper ... ...des dissolving of 100mg of PC into 15 ml ethanol and then this solution mixture is added drop-wise into a Vitamin C solution. Continuous stirring is required. The conditions like low temperature and moisture content can be achieved. The organic solvent is then evaporated and by maintaining pH at 7.4 of the phosphate buffer solution (PBS), the solvent traces are removed. The Liposome dispersion is then stored under vacuum overnight. The liposome size can be downsized by sonication. Liposome characterisation i.e. size and surface structure can be observed using cryo-transmission electron microscopy (cryo-TEM) (27). The main disadvantage of liposomes is leakage of encapsulated material. Their solubility is relatively low and requires other solubilizers during formulation, which ultimately leads to higher production cost. Another drawback is their shorter half-life(28).

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