Acute and Subacute Toxicity of Sorbitan Monostearate (Span 60) Non-ionic Surfactant Vesicles (Niosomes) in Sprague Dawley Rats

2016 ◽  
Vol 14 (2) ◽  
pp. 1-9 ◽  
Author(s):  
Jankie Satish ◽  
Johnson Jenelle ◽  
Pinto-Pereira Lexley ◽  
Adebayo Amusa ◽  
Pillai Gopalakrishna
2015 ◽  
Vol 4 (4) ◽  
pp. 316-321 ◽  
Author(s):  
Narhari Das ◽  
Durajan Goshwami ◽  
Md. Sharif Hasan ◽  
Sheikh Zahir Raihan

2020 ◽  
Vol 9 (4) ◽  
pp. 265-269
Author(s):  
Toonse Mudimba ◽  
◽  
James Mbaria ◽  
Timothy Maitho ◽  
Tafadzwa Taderera ◽  
...  

2011 ◽  
Vol 51 (09) ◽  
pp. 769-774 ◽  
Author(s):  
Se-Kwon Kim ◽  
Pyo-Jam Park ◽  
Hyun-Pil Yang ◽  
Sang-Sup Han

2020 ◽  
Vol 6 (1) ◽  
pp. 21-26
Author(s):  
Kartika Zulfa ◽  
◽  
Ferri Widodo ◽  
Oktavia Eka Puspita ◽  
◽  
...  

Excessive radiation from UV light can cause skin damage to melanoma, especially UVB rays. Chronic effects from exposure of excessive UVB rays can induce gene mutations because the exposure of excessive UVB rays directly causes damage to cellular DNA by producing ROS in the epidermis, dermis, and skin epithelium cells. The use of sunscreen is very necessary to prevent skin damage. Sunscreen containing antioxidants are highly recommended to protect the skin from free radicals UVB rays. Pterostilbene is one of the phenolic compounds, which has the pharmacological activity of antioxidants and UV filters to be one of the recommended compounds for sunscreen components. A good delivery system is needed to be formulated to improve the pharmacological effects of pterostilbene on topical use. Niosomes are non-ionic surfactant vesicles which are one of the amphiphilic carrier systems which can carry hydrophobic active ingredients such as pterostilbene, which are expected to increase the pharmacological effect by increasing the penetration of pterostilbene into the skin. Pterostilbene niosome using non-ionic surfactant (span 80 and span 60) by thin layer hydration method. The research aimed to examine the effect of surfactant concentration (span 80 and span 60) 2, 4, and 6 g toward the characterization of niosome pterostilbene and determine the optimum formulation by particle size. The results of the study showed that the particle size was smaller with an increase in span concentration. Based on these results, the optimum formulation of pterostilbene niosomes is obtained using span 60 with a concentration of 6 g.


2015 ◽  
Vol 31 (4) ◽  
pp. 403-414 ◽  
Author(s):  
Chung-Tack Han ◽  
Myoung-Jun Kim ◽  
Seol-Hee Moon ◽  
Yu-Rim Jeon ◽  
Jae-Sik Hwang ◽  
...  

2019 ◽  
Vol 238 ◽  
pp. 111852
Author(s):  
Eunsook Park ◽  
Mee-Young Lee ◽  
Chang-Seob Seo ◽  
Hyeun-Kyoo Shin ◽  
Su-Cheol Han ◽  
...  

2000 ◽  
Vol 38 (8) ◽  
pp. 679-688 ◽  
Author(s):  
G.B Janssen ◽  
R.B Beems ◽  
G.J.A Speijers ◽  
H.P van Egmond

2010 ◽  
Vol 30 (8) ◽  
pp. 952-964 ◽  
Author(s):  
V. Gayathri ◽  
V. Muthulakshmi ◽  
C. Chandronitha ◽  
M. Vasanthkumar ◽  
G. Ramakrishnan ◽  
...  

Sirupeellai samoola kudineer (SK), a polyherbal decoction, has been used in Siddha system of medicine for the management of Urolithiasis. Since, there exists no documentation of preclinical toxicological evaluation of SK earlier, in the present study, acute and subacute toxicity of SK was assessed in Sprague Dawley rats as per OECD guideline 423 and 407, respectively. In the acute toxicity study, SK did not produce any toxic signs at a dose level of 50 ml/kg b.wt/p.o. Three doses of SK (4.5, 9.0, 18.0 ml/kg b.wt) were administered and observed for various behavioral, physiological, biochemical, and haematological changes for 28 days in the subacute toxicity study. Low and mid dose of SK (4.5 and 9.0 ml/kg b.wt) did not exhibit any significant physiological and haematological alterations. Whereas, high dose (18.0 ml/kg bw) treatment exhibited significant changes in creatinine, gamma glutamyl transferase (GGT) and acid phosphatase (ACP) levels in serum. Further, histopathological examinations of brain, heart, liver, kidney and sex organs revealed normal architecture signifying no morphological changes upto a dose of 9.0 ml/kg. However, 18.0 ml/kg of SK administration showed few histopathological changes as compared to the control. Based on these results, it can be concluded that Sirupeellai samoola kudineer is safe and non-toxic upto 9.0 ml/kg for 28 days in experimental rats.


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