1.Anti cataract potential of phyllanthus niruri in galactose induced cataractogenesis of rat
Suresh Kumar GUPTA ; Vivekanandhan KALAISELVAN ; Ashish SHARMA ; Sushma SRIVASTAVA ; Shyam Sunder AGRAWAL
International Eye Science 2009;9(6):1011-1015
AIM: To evaluate anti cataract effect of phyllanthus niruri (PN) both in vitro and in vivo galactose induced cataract.METHODS: Aqueous extract of PN was evaluated against galactose-induced cataract both in vitro and in vivo. Galactosaemic cataract was induced in rats by feeding 300g/L galactose diet. PN was administered orally at three-dose levels 75, 150 and 300 mg/kg of body weight. Rat lenses were subjected to osmotic stress in vitro by incorporating galactose (30mmol/L) in the culture medium. The effect of PN (720 and 880μg/mL) on the glutathione (GSH) and polyols levels was studied.RESULTS: PN significantly delayed the onset and progression of cataract in vivo. In addition to the delay in reaching various stages of development of cataract, stage IV did not develop with lower doses till the completion of experimental period. Lenses treated with PN 880μg/mL concentration showed higher levels of GSH and decreased levels of polyols in vitro. In vivo, 75mg/kg significantly delayed the onset and progression of cataract as compared to control.CONCLUSION: PN delayed the process of cataracto-genesis in the experimental models. However, further study is required to extrapolate the use in human beings for the prevention of cataract.
2.Small interfering RNA for cancer treatment: overcoming hurdles in delivery.
Nitin Bharat CHARBE ; Nikhil D AMNERKAR ; B RAMESH ; Murtaza M TAMBUWALA ; Hamid A BAKSHI ; Alaa A A ALJABALI ; Saurabh C KHADSE ; Rajendran SATHEESHKUMAR ; Saurabh SATIJA ; Meenu METHA ; Dinesh Kumar CHELLAPPAN ; Garima SHRIVASTAVA ; Gaurav GUPTA ; Poonam NEGI ; Kamal DUA ; Flavia C ZACCONI
Acta Pharmaceutica Sinica B 2020;10(11):2075-2109
In many ways, cancer cells are different from healthy cells. A lot of tactical nano-based drug delivery systems are based on the difference between cancer and healthy cells. Currently, nanotechnology-based delivery systems are the most promising tool to deliver DNA-based products to cancer cells. This review aims to highlight the latest development in the lipids and polymeric nanocarrier for siRNA delivery to the cancer cells. It also provides the necessary information about siRNA development and its mechanism of action. Overall, this review gives us a clear picture of lipid and polymer-based drug delivery systems, which in the future could form the base to translate the basic siRNA biology into siRNA-based cancer therapies.