Literature DB >> 21803597

Synthesis and evaluation of novel tetrapropoxycalix[4]arene enones and cinnamates for protection from ultraviolet radiation.

H M Chawla1, Nalin Pant, Satish Kumar, Sarika Mrig, Bindu Srivastava, Naresh Kumar, D Stc Black.   

Abstract

A series of novel calix[4]arene enones (5-7) and cinnamates (12-14) have been synthesized and evaluated for ensuring protection from ultraviolet radiation (UVR). Spectroscopic analyses has revealed that compound 6 absorbs ultraviolet radiations between 280 and 350 nm with an absorption maximum at 312 nm. Its molar absorption coefficient (ε) (>5 × 10(4)M(-1)cm(-1)) and bandwidth are larger than those for the commercially used sun protectants (oxybenzone (OB), 2-ethylhexyl 4-methoxycinnamate (OMC) and avobenzone). The in vitro Sun Protection Factor (SPF) measurement revealed an SPF of 5.2 at 2% concentration of 6 in home made emulsion formulations while combination of 2% each of 6 and OMC gave an SPF of 8.8. Lower sun protection seems to be compensated by significant protection from more harmful UVA radiations (UVA/UVB absorbance ratio of 0.62).
Copyright © 2011. Published by Elsevier B.V.

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Year:  2011        PMID: 21803597     DOI: 10.1016/j.jphotobiol.2011.06.007

Source DB:  PubMed          Journal:  J Photochem Photobiol B        ISSN: 1011-1344            Impact factor:   6.252


  1 in total

1.  Supramolecular interaction of two tryptophans with p-sulfonated calix[4,6,8]arene.

Authors:  Tao-Tao Pang; Hai-Long Liu; Li-Ming Du; Yin-Xia Chang; Yun-Long Fu
Journal:  J Fluoresc       Date:  2013-07-31       Impact factor: 2.217

  1 in total

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