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<br /><br />From its use in topical medication and from limited information from occupational research, resorcinol doesn't seem like irritating to the pores and skin in the concentrations reported. Van Leeuwen et al. There is no indication as as to if the teratogenic effects had been endocrine mediated or not EC, c. In people, dermal exposure to resorcinol has been reported to be associated with thyroid effects, CNS disturbances, pink blood cell adjustments, and a low incidence of pores and skin sensitization. Five of three.<br />The bulk of the urine-recovered dye will need to have been taken up into the sexy layer of the pores and skin after which slowly released into the circulation. A cumulative four-day absorption assuming cm 2 of scalp was given as zero.<br /><br />Although thyroid effects are a major finish-level in each human case-studies and animal research, there is a lack of consistency in the leads to the animal research. Resorcinol caused no antagonistic results in several replica and developmental toxicity research in rats and rabbits. Resorcinol is not thought of to be genotoxic.<br />Other skin results have been hyperplasia, hyperkeratosis, irritation, and sebaceous gland hyperplasia, whereas there were no systemic remedy-associated lesions. With resorcinol, a number of initiation—promotion research with hamsters Maruyama et al. Female Syrian golden hamsters 10—20 per group had been handled with two subcutaneous injections of. In a examine carried out by Hasegawa et al.<br />These figures agree properly with the above publicity estimate based on the Yeung et al.<br /><br /><h1></h1><br /><br /><ul><br />  <br />  <br />  <br /> <li>Exposure to resorcinol by way of peeling agents presents an acute exposure state of affairs where the person is uncovered to a high concentration 7.</li><br /> <br /> <br /> <br /> <li>There had been no published animal studies displaying thyroidal effects with a dose—response relationship that could be used for a tolerable consumption.</li><br />  <br />  <br />  <br /> <li>Resorcinol triggered no adverse results in a number of replica and developmental toxicity research in rats and rabbits.</li><br />  <br />  <br /> <br /> <li>As talked about in part 9.</li><br />  <br />  <br /> <br /> <li>Data concerning the completely different job categories were not offered.</li><br /> <br /> <br /> <br /></ul><br />In in vitro genotoxicity tests, resorcinol showed largely negative outcomes. Results from all reported in vivo exams for genotoxicity had been unfavorable. Mostly negative results had been reported in the initiation—promotion studies performed using a number of species. UV irradiation caused no elevated pores and skin reactions. The iodination process is catalysed by a haem-containing enzyme.<br />In both species, there were no adverse results on ultimate imply body weights, haematology, or clinical chemistry parameters, and no chemical-related gross or microscopic lesions had been noticed. In another examine, rats have been exposed to 0 or zero. No thyroid hormone measurements were carried out.<br />The acute dermal toxicity of resorcinol was studied in male albino rabbits Koppers Company, Signs of intoxication included salivation, tremors, and convulsions, and treated skin areas confirmed slight erythema and excessive dryness. Mean knowledge for 3 donors and sixteen replicates indicate a plateau in receptor fluid concentration between 24 and 48 h, as reflected by cumulative absorption values of 1. A regular-state permeability coefficient. For male albino rats strain not given;.<br />A concentration of 0. These substances had been found to be potent inhibitors of thyroid peroxidase or I organification. Resorcinol as well as 2- and 5-methylresorcinol had been reported to be At an iodide concentration of 0.<br />In one other study, male F rats have been handled with three intraperitoneal injections of three-methyl-. Based on the examine of Yeung et al.<br /><br /><h2></h2><br />The tolerable intake of 0. It is therefore potential that these neurological effects are because of the acute impact of the gavage administration. CNS results in people and animals have been associated with acute publicity to resorcinol.<br /><br /><h3></h3><br />According to the outcomes obtained, Daphnia magna is the most delicate organism, and resorcinol can be categorised as acutely toxic only to Daphnia. However, this value is questionable for use as a limit worth in threat assessment this is the highest concentration tested in this research , and the NOEC could be significantly greater than said in the examine. In the environment, resorcinol is quickly degraded half-life about 2 h by response with photochemically produced hydroxyl radicals. Under aerobic conditions, resorcinol proved to be readily biodegradable in a test conducted based on OECD TG C, and it's prone to be biodegraded beneath anaerobic situations.

Revision as of 23:19, 11 March 2020



From its use in topical medication and from limited information from occupational research, resorcinol doesn't seem like irritating to the pores and skin in the concentrations reported. Van Leeuwen et al. There is no indication as as to if the teratogenic effects had been endocrine mediated or not EC, c. In people, dermal exposure to resorcinol has been reported to be associated with thyroid effects, CNS disturbances, pink blood cell adjustments, and a low incidence of pores and skin sensitization. Five of three.
The bulk of the urine-recovered dye will need to have been taken up into the sexy layer of the pores and skin after which slowly released into the circulation. A cumulative four-day absorption assuming cm 2 of scalp was given as zero.

Although thyroid effects are a major finish-level in each human case-studies and animal research, there is a lack of consistency in the leads to the animal research. Resorcinol caused no antagonistic results in several replica and developmental toxicity research in rats and rabbits. Resorcinol is not thought of to be genotoxic.
Other skin results have been hyperplasia, hyperkeratosis, irritation, and sebaceous gland hyperplasia, whereas there were no systemic remedy-associated lesions. With resorcinol, a number of initiation—promotion research with hamsters Maruyama et al. Female Syrian golden hamsters 10—20 per group had been handled with two subcutaneous injections of. In a examine carried out by Hasegawa et al.
These figures agree properly with the above publicity estimate based on the Yeung et al.







  • Exposure to resorcinol by way of peeling agents presents an acute exposure state of affairs where the person is uncovered to a high concentration 7.




  • There had been no published animal studies displaying thyroidal effects with a dose—response relationship that could be used for a tolerable consumption.




  • Resorcinol triggered no adverse results in a number of replica and developmental toxicity research in rats and rabbits.




  • As talked about in part 9.




  • Data concerning the completely different job categories were not offered.





In in vitro genotoxicity tests, resorcinol showed largely negative outcomes. Results from all reported in vivo exams for genotoxicity had been unfavorable. Mostly negative results had been reported in the initiation—promotion studies performed using a number of species. UV irradiation caused no elevated pores and skin reactions. The iodination process is catalysed by a haem-containing enzyme.
In both species, there were no adverse results on ultimate imply body weights, haematology, or clinical chemistry parameters, and no chemical-related gross or microscopic lesions had been noticed. In another examine, rats have been exposed to 0 or zero. No thyroid hormone measurements were carried out.
The acute dermal toxicity of resorcinol was studied in male albino rabbits Koppers Company, Signs of intoxication included salivation, tremors, and convulsions, and treated skin areas confirmed slight erythema and excessive dryness. Mean knowledge for 3 donors and sixteen replicates indicate a plateau in receptor fluid concentration between 24 and 48 h, as reflected by cumulative absorption values of 1. A regular-state permeability coefficient. For male albino rats strain not given;.
A concentration of 0. These substances had been found to be potent inhibitors of thyroid peroxidase or I organification. Resorcinol as well as 2- and 5-methylresorcinol had been reported to be At an iodide concentration of 0.
In one other study, male F rats have been handled with three intraperitoneal injections of three-methyl-. Based on the examine of Yeung et al.


The tolerable intake of 0. It is therefore potential that these neurological effects are because of the acute impact of the gavage administration. CNS results in people and animals have been associated with acute publicity to resorcinol.


According to the outcomes obtained, Daphnia magna is the most delicate organism, and resorcinol can be categorised as acutely toxic only to Daphnia. However, this value is questionable for use as a limit worth in threat assessment this is the highest concentration tested in this research , and the NOEC could be significantly greater than said in the examine. In the environment, resorcinol is quickly degraded half-life about 2 h by response with photochemically produced hydroxyl radicals. Under aerobic conditions, resorcinol proved to be readily biodegradable in a test conducted based on OECD TG C, and it's prone to be biodegraded beneath anaerobic situations.