| Literature DB >> 20207391 |
Mohamed Nassef1, Sang Gyoon Kim, Masanori Seki, Ik Joon Kang, Takeshi Hano, Yohei Shimasaki, Yuji Oshima.
Abstract
We examined the toxicity of three pharmaceuticals and personal care products (PPCPs) - triclosan (TCS), diclofenac (DCF), and carbamazepine (CBMZ) - on embryonic development of Japanese medaka (Oryzias latipes) using in ovo nanoinjection. Medaka eggs (8h post-fertilization; late blastula stage) were injected with 0.5nL of triolein (vehicle control) or 0.5nL of PPCPs, using different doses of TCS (1, 5, or 9ng), DCF (1, 5, or 12ng), or CBMZ (1, 5, or 12ng) per egg in triolein, in addition to uninjected control. Following injection, we recorded survival, embryonic lesions, delay in embryonic development (eye, embryonic body and internal organs), heart beat rate, hatchability, and hatching time of embryos and upward swimming of larvae. As a result, injected PPCPs caused toxic responses to medaka embryos during embryonic development and around the day of hatching. Based on estimated EC(50) values of PPCPs doses on survival of injected embryos at hatching, TCS (at a dose of 4.2ngegg(-1)) was generally more toxic to medaka embryos, followed by DCF (6.0ngegg(-1)), and CBMZ (13.1ngegg(-1)). We conclude that the nanoinjection medaka embryos model is a valuable tool for analyzing the effects of chemicals on the development of fish embryos and feasibility of nanoinjecting PPCPs into small fish eggs perhaps mimicking early exposure resulting from oocyte uptake of contaminants from maternal extra gonadal tissues. Copyright 2010 Elsevier Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20207391 DOI: 10.1016/j.chemosphere.2010.02.002
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086