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2.
Food Chem Toxicol ; 159 Suppl 1: 112715, 2022 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-34848254

RESUMEN

The Research Institute for Fragrance Materials, Inc. (RIFM) has evaluated safety data for fragrance materials for 55 years. The safety assessment of Natural Complex Substances (NCS) is similar to that of discrete fragrance materials; all of the same endpoints are evaluated. A series of decision trees, reflecting advances in risk assessment approaches of mixtures and toxicological methodologies, follows a tiered approach for each endpoint using a 4-step process with testing only as a last resort: 1) evaluate available data on NCS; 2) verify whether the Threshold of Toxicological Concern (TTC) can be applied; 3) verify whether the NCS risk assessment can be achieved on a component basis; and 4) determine whether data must be generated. Using in silico tools, RIFM examined NCS similarities based on the plant part, processing, and composition of materials across 81 plant families to address data gaps. Data generated from the Creme RIFM Aggregate Exposure Model for over 900 fragrance NCS demonstrate that dermal exposure is the primary route of human exposure for NCS fragrance uses. Over a third of materials are below the most conservative TTC limits. This process aims to provide a comprehensive Safety Assessment of NCS used as a fragrance ingredient.


Asunto(s)
Exposición a Riesgos Ambientales/efectos adversos , Odorantes/análisis , Perfumes/toxicidad , Extractos Vegetales/efectos adversos , Plantas/química , Seguridad , Piel , Academias e Institutos , Administración Cutánea , Animales , Mezclas Complejas , Árboles de Decisión , Dermatitis Fototóxica , Determinación de Punto Final , Humanos , Pruebas de Mutagenicidad , Perfumes/análisis , Extractos Vegetales/química , Sistema de Registros , Medición de Riesgo , Piel/efectos de los fármacos
3.
Food Chem Toxicol ; 134 Suppl 2: 111024, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31812735

RESUMEN

Hydroxycitronellal dimethyl acetal was evaluated for genotoxicity, repeated dose toxicity, reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, and environmental safety. Data from read-across analog hydroxycitronellal diethyl acetal (CAS # 7779-94-4) show that hydroxycitronellal dimethyl acetal is not expected to be genotoxic. The repeated dose, reproductive, and local respiratory toxicity endpoints were evaluated using the TTC for a Cramer Class I material and the exposure to hydroxycitronellal dimethyl acetal is below the TTC (0.03 mg/kg/day, 0.03 mg/kg/day, and 1.4 mg/day, respectively). Data from hydroxycitronellal dimethyl acetal and from read-across material hydroxycitronellal diethyl acetal (CAS # 7779-94-4) show that there are no safety concerns for skin sensitization under the current declared levels of use. The phototoxicity/photoallergenicity endpoints were evaluated based on UV spectra; hydroxycitronellal dimethyl acetal is not expected to be phototoxic/photoallergenic. The environmental endpoints were evaluated; hydroxycitronellal dimethyl acetal was found not to be PBT as per the IFRA Environmental Standards, and its risk quotients, based on its current volume of use in Europe and North America (i.e., PEC/PNEC), are <1.


Asunto(s)
Acetales/toxicidad , Octanoles/toxicidad , Odorantes , Acetales/química , Animales , Seguridad de Productos para el Consumidor , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Escherichia coli/efectos de los fármacos , Humanos , Pruebas de Mutagenicidad , Nivel sin Efectos Adversos Observados , Octanoles/química , Medición de Riesgo , Salmonella typhimurium/efectos de los fármacos
4.
Food Chem Toxicol ; 134 Suppl 2: 111002, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31785315

RESUMEN

The existing information supports the use of this material as described in this safety assessment. p-Tolyl acetate was evaluated for genotoxicity, repeated dose toxicity, reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, and environmental safety. Data from read-across analog ethyl p-tolyl carbonate (CAS # 22719-81-9) show that p-tolyl acetate is not expected to be genotoxic. Data on read-across materials p-cresol (CAS # 106-44-5) and acetic acid (CAS # 64-19-7) provide a calculated MOE >100 for the repeated dose and reproductive toxicity endpoints. The skin sensitization endpoint was completed using DST for reactive materials (64 µg/cm2); exposure is below the DST. The phototoxicity/photoallergenicity endpoints were evaluated based on UV spectra; p-tolyl acetate is not expected to be phototoxic/photoallergenic. The local respiratory toxicity endpoint was evaluated using the TTC for a Cramer Class I material, and the exposure to p-tolyl acetate is below the TTC (1.4 mg/day).The environmental endpoints were evaluated; p-tolyl acetate was found not to be PBT as per the IFRA Environmental Standards, and its risk quotients, based on its current volume of use in Europe and North America (i.e., PEC/PNEC), are <1.


Asunto(s)
Cresoles/toxicidad , Odorantes , Animales , Seguridad de Productos para el Consumidor , Cresoles/química , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Escherichia coli/efectos de los fármacos , Humanos , Pruebas de Mutagenicidad , Nivel sin Efectos Adversos Observados , Medición de Riesgo , Salmonella typhimurium/efectos de los fármacos
5.
Food Chem Toxicol ; 134 Suppl 2: 110948, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31756354

RESUMEN

The existing information supports the use of this material as described in this safety assessment. 4-(p-Hydroxyphenyl)-2-butanone was evaluated for genotoxicity, repeated dose toxicity, developmental and reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, and environmental safety. Data show that 4-(p-hydroxyphenyl)-2-butanone is not genotoxic. Data on 4-(p-hydroxyphenyl)-2-butanone provide a calculated MOE >100 for the repeated dose toxicity endpoint. The developmental and reproductive toxicity and local respiratory toxicity endpoints were evaluated using the TTC for a Cramer Class I material, and the exposure to 4-(p-hydroxyphenyl)-2-butanone is below the TTC (0.03 mg/kg/day and 1.4 mg/day, respectively). Data from 4-(p-hydroxyphenyl)-2-butanone show that there are no safety concerns for skin sensitization under the current declared levels of use. The phototoxicity/photoallergenicity endpoints were evaluated based on UV spectra; 4-(p-hydroxyphenyl)-2-butanone is not expected to be phototoxic/photoallergenic. The environmental endpoints were evaluated; 4-(p-hydroxyphenyl)-2-butanone was found not to be PBT as per the IFRA Environmental Standards, and its risk quotients, based on its current volume of use in Europe and North America (i.e., PEC/PNEC), are <1.


Asunto(s)
Butanonas/toxicidad , Odorantes , Animales , Butanonas/química , Seguridad de Productos para el Consumidor , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Humanos , Pruebas de Mutagenicidad , Nivel sin Efectos Adversos Observados , Medición de Riesgo , Salmonella typhimurium/efectos de los fármacos
6.
Food Chem Toxicol ; 134 Suppl 2: 110999, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31783104

RESUMEN

The existing information supports the use of this material as described in this safety assessment. Isobutyl alcohol was evaluated for genotoxicity, repeated dose toxicity, reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, and environmental safety. Data show that isobutyl alcohol is not genotoxic. Data on isobutyl alcohol provide a calculated MOE >100 for the repeated dose toxicity and reproductive toxicity endpoints. Data from read-across material isoamyl alcohol (CAS # 123-51-3) show that there are no safety concerns for isobutyl alcohol for skin sensitization under the current declared levels of use. The phototoxicity/photoallergenicity endpoints were evaluated based on UV spectra; isobutyl alcohol is not expected to be phototoxic/photoallergenic. The local respiratory toxicity endpoint was evaluated using the TTC for a Cramer Class I material and the exposure to isobutyl alcohol is below the TTC (1.4 mg/day). The environmental endpoints were evaluated; isobutyl alcohol was found not to be PBT as per the IFRA Environmental Standards, and its risk quotients, based on its current volume of use in Europe and North America (i.e., PEC/PNEC), are <1.


Asunto(s)
Butanoles/toxicidad , Odorantes , Animales , Butanoles/química , Seguridad de Productos para el Consumidor , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Humanos , Pruebas de Mutagenicidad , Nivel sin Efectos Adversos Observados , Medición de Riesgo , Salmonella typhimurium/efectos de los fármacos
7.
Food Chem Toxicol ; 134 Suppl 2: 110825, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31542434

RESUMEN

Methyl 2-octynoate was evaluated for genotoxicity, repeated dose toxicity, developmental and reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, and environmental safety. Data show that methyl 2-octynoate is not genotoxic. Data provided methyl 2-octynoate a NESIL of 110 µg/cm2 for the skin sensitization endpoint. The repeated dose, developmental and reproductive, and local respiratory toxicity endpoints were evaluated using the TTC for a Cramer Class II material, and the exposure to methyl 2-octynoate is below the TTC (0.009 mg/kg/day, 0.009 mg/kg/day, and 0.47 mg/day, respectively). The phototoxicity/photoallergenicity endpoints were evaluated based on UV spectra; methyl 2-octynoate is not expected to be phototoxic/photoallergenic. The environmental endpoints were evaluated; methyl 2-octynoate was found not to be PBT as per the IFRA Environmental Standards, and its risk quotients, based on its current volume of use in Europe and North America (i.e., PEC/PNEC), are <1.


Asunto(s)
Caprilatos/toxicidad , Odorantes , Animales , Caprilatos/química , Seguridad de Productos para el Consumidor , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Humanos , Pruebas de Mutagenicidad , Nivel sin Efectos Adversos Observados , Medición de Riesgo , Salmonella typhimurium/efectos de los fármacos
8.
Food Chem Toxicol ; 134 Suppl 2: 110716, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31365887

RESUMEN

Methyl ionone (mixture of isomers) was evaluated for genotoxicity, repeated dose toxicity, developmental and reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, and environmental safety. Data from methyl ionone (mixture of isomers) show that the material is not genotoxic and provided a NESIL of 70,000 µg/cm2 for the skin sensitization endpoint. Data provided a calculated MOE >100 for the repeated dose toxicity and developmental toxicity endpoints, and data from read-across material (E)-ß-ionone (CAS # 79-77-6) provided a calculated MOE >100 for the reproductive toxicity endpoint. For the local respiratory endpoint, a calculated MOE >100 was provided by the read-across material ß-ionone (CAS # 14901-07-6). The phototoxicity/photoallergenicity endpoints were evaluated based on data and UV spectra; the material is not phototoxic/photoallergenic. The environmental endpoints were evaluated with data from the target chemical and read-across material α-allylionone (CAS # 79-78-7), and the material was not found to be PBT; its risk quotients, based on current volume of use in Europe and North America (PEC/PNEC), are <1.


Asunto(s)
Odorantes , Terpenos/toxicidad , Animales , Línea Celular , Seguridad de Productos para el Consumidor , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Escherichia coli/efectos de los fármacos , Humanos , Isomerismo , Pruebas de Mutagenicidad , Nivel sin Efectos Adversos Observados , Medición de Riesgo , Salmonella typhimurium/efectos de los fármacos , Terpenos/química
9.
Food Chem Toxicol ; 130 Suppl 1: 110622, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31238136

RESUMEN

The existing information supports the use of this material as described in this safety assessment. Methyl 2-nonenoate was evaluated for genotoxicity, repeated dose toxicity, reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, and environmental safety. Data from read-across analog ethyl trans-2,cis-4-decadienoate (CAS # 3025-30-7) show that methyl 2-nonenoate is not expected to be genotoxic. The repeated dose, reproductive, and local respiratory toxicity endpoints were evaluated using the TTC for a Cramer Class I material, and the exposure to methyl 2-nonenoate is below the TTC (0.03 mg/kg/day, 0.03 mg/kg/day, and 1.4 mg/day, respectively). Data from the target and read-across analog isobutyl-2-butenoate (CAS # 589-66-2) do not indicate the material is a sensitizer. The phototoxicity/photoallergenicity endpoints were evaluated based on data and UV spectra; methyl 2-nonenoate is not expected to be phototoxic/photoallergenic. The environmental endpoints were evaluated; methyl 2-nonenoate was found not to be PBT as per the IFRA Environmental Standards, and its risk quotients, based on its current volume of use in Europe and North America (i.e., PEC/PNEC), are <1.


Asunto(s)
Ácidos Grasos Monoinsaturados/química , Ácidos Grasos Monoinsaturados/toxicidad , Perfumes/química , Perfumes/toxicidad , Pruebas de Toxicidad/métodos , Animales , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Humanos , Estructura Molecular , Medición de Riesgo
10.
Food Chem Toxicol ; 130 Suppl 1: 110607, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31233870

RESUMEN

The existing information supports the use of this material as described in this safety assessment. Isobutyl propionate was evaluated for genotoxicity, repeated dose toxicity, reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, and environmental safety. Data from read-across analog isobutyl acetate (CAS # 110-19-0) show that isobutyl propionate is not expected to be genotoxic. Data from read-across analog isoamyl acetate (CAS # 123-92-2) show that there are no safety concerns for isobutyl propionate for skin sensitization under the current declared levels of use. The repeated dose and reproductive endpoints were evaluated using the TTC for a Cramer Class I material, and the exposure to isobutyl propionate is below the TTC (0.03 mg/kg/day and 0.03 mg/kg/day, respectively). For the local respiratory endpoint, a calculated MOE >100 was provided by read-across analog butyl acetate (CAS # 123-86-4). The phototoxicity/photoallergenicity endpoints were evaluated based on UV spectra; isobutyl propionate is not expected to be phototoxic/photoallergenic. The environmental endpoints were evaluated; isobutyl propionate is not PBT as per the IFRA Environmental Standards. For the risk assessment, isobutyl propionate was not able to be risk screened as there were no reported volumes of use for North America or Europe in the 2015 IFRA Survey.


Asunto(s)
Perfumes/química , Perfumes/toxicidad , Propionatos/química , Propionatos/toxicidad , Pruebas de Toxicidad/métodos , Animales , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Humanos , Estructura Molecular , Medición de Riesgo
11.
Food Chem Toxicol ; 130 Suppl 1: 110588, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31216429

RESUMEN

There are insufficient toxicity data on the target material propanal diethyl acetal (CAS # 4744-08-5). Hence, in silico evaluation was conducted to determine read-across analogs for this material. Based on structural similarity, reactivity, metabolism data, physical-chemical properties, and expert judgment, analogs acetal (CAS # 105-57-7) and butane, 1,1'-[methylenebis(oxy)]bis- (CAS # 2568-90-3) were identified as read-across materials with sufficient data for toxicological evaluation of genotoxicity.


Asunto(s)
Cetonas/química , Perfumes/química , Perfumes/toxicidad , Pruebas de Toxicidad/métodos , Animales , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Humanos , Estructura Molecular , Medición de Riesgo
13.
Food Chem Toxicol ; 97S: S192-S200, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27697541

RESUMEN

: The use of this material under current conditions is supported by existing information. This material was evaluated for genotoxicity, repeated dose toxicity, developmental and reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, as well as environmental safety. Data show that this material is not genotoxic nor does it have skin sensitization potential. The local respiratory toxicity endpoint was completed using the TTC (Threshold of Toxicological Concern) for a Cramer Class I material (1.4 mg/day). The repeated dose toxicity endpoint was completed using ethylene dodecanedioate (CAS # 54982-83-1) as a suitable read across analog, which provided a MOE > 100. The developmental and reproductive toxicity endpoint was completed using oxacyclohexadec-12-en-2-one, (12E)- (CAS # 111879-80-2) as a suitable read across analog, which provided a MOE > 100. The phototoxicity/photoallergenicity endpoint was completed based on suitable UV spectra along with data on the target material. The environmental endpoint was completed as described in the RIFM Framework along with data on the suitable read across analog oxacyclohexadec-12-en-2-one, (12E)- (CAS # 111879-80-2).


Asunto(s)
Éteres Cíclicos/toxicidad , Perfumes/toxicidad , Pruebas de Toxicidad/métodos , Animales , Seguridad de Productos para el Consumidor , Daño del ADN/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Éteres Cíclicos/química , Nivel sin Efectos Adversos Observados , Perfumes/química , Ratas , Medición de Riesgo
18.
Food Chem Toxicol ; 97S: S147-S156, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27600295

RESUMEN

The use of this material under current conditions is supported by existing information. This material was evaluated for genotoxicity, repeated dose toxicity, developmental toxicity, reproductive toxicity, local respiratory toxicity, phototoxicity, skin sensitization, as well as environmental safety. Data show that this material is not genotoxic. Data from the suitable read across analog 2-butyloctan-1-ol (CAS # 3913-02-8) show that this material does not have skin sensitization potential. The reproductive and local respiratory toxicity endpoints were completed using the TTC (Threshold of Toxicological Concern) for a Cramer Class I material (0.03 and 1.4 mg/day, respectively). The developmental and repeat dose toxicity endpoints were completed data on the target material which provided a MOE > 100. The phototoxicity/photoallergenicity endpoint was completed based on suitable UV spectra. The environmental endpoint was completed as described in the RIFM Framework.


Asunto(s)
Hexanoles/toxicidad , Perfumes/toxicidad , Plastificantes/toxicidad , Pruebas de Toxicidad/métodos , Animales , Seguridad de Productos para el Consumidor , Daño del ADN/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Hexanoles/química , Nivel sin Efectos Adversos Observados , Perfumes/química , Plastificantes/química , Ratas , Medición de Riesgo
19.
Food Chem Toxicol ; 97S: S157-S167, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27658323

RESUMEN

The use of this material under current conditions is supported by existing information. This material was evaluated for genotoxicity, repeated dose toxicity, developmental and reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, as well as environmental safety. Data from the suitable read across analog 2-ethylhexanol (CAS # 104-76-7) show that this material is not genotoxic. Data from the suitable read across analog isopropyl alcohol (CAS # 67-63-0) show that this material does not have skin sensitization potential. The local respiratory toxicity endpoint was completed using the TTC (Threshold of Toxicological Concern) for a Cramer Class I material (1.4 mg/day). The repeated dose toxicity endpoint was completed using 2-ethylhexanol (CAS # 104-76-7) and 1-heptanol, 2-propyl (CAS # 10042-59-8) as suitable read across analogs, which provided a MOE > 100. The developmental and reproductive toxicity endpoint was completed using 2-ethyl-hexanol (CAS # 104-76-7) and isobutyl alcohol (CAS # 78-83-1) as suitable read across analogs, which provided a MOE > 100. The phototoxicity/photoallergenicity endpoint was completed based on suitable UV spectra. The environmental endpoint was completed as described in the RIFM Framework.


Asunto(s)
Hexanoles/toxicidad , Perfumes/toxicidad , Pruebas de Toxicidad/métodos , Animales , Seguridad de Productos para el Consumidor , Daño del ADN/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Hexanoles/química , Nivel sin Efectos Adversos Observados , Perfumes/química , Ratas , Medición de Riesgo
20.
Food Chem Toxicol ; 97S: S168-S179, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-27663839

RESUMEN

The use of this material under current conditions is supported by existing information. This material was evaluated for genotoxicity, repeated dose toxicity, developmental and reproductive toxicity, local respiratory toxicity, phototoxicity/photoallergenicity, skin sensitization, as well as environmental safety. Data from the suitable read across analog linalool (CAS # 78-70-6) show that this material is not genotoxic nor does it have skin sensitization potential and also provided a MOE > 100 for the local respiratory endpoint. The repeated dose, developmental and reproductive toxicity endpoints were completed using nerolidol (isomer unspecified, CAS # 7212-44-4) as a suitable read across analog, which provided a MOE > 100. The phototoxicity/photoallergenicity endpoint was completed based on suitable UV spectra. The environmental endpoint was completed as described in the RIFM Framework.


Asunto(s)
Alcoholes Grasos/toxicidad , Perfumes/toxicidad , Pruebas de Toxicidad/métodos , Animales , Seguridad de Productos para el Consumidor , Daño del ADN/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Determinación de Punto Final , Alcoholes Grasos/química , Nivel sin Efectos Adversos Observados , Perfumes/química , Ratas , Medición de Riesgo
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