N-Methyl-N'-Nitroguanidine: Irritation, Sensitization, and Acute Oral Toxicity, Genotoxicity, and Methods for Analysis in Biological Samples

1993 ◽  
Vol 9 (3) ◽  
pp. 457-477 ◽  
Author(s):  
E.R. Kinkead ◽  
R.E. Wolfe ◽  
S.A. Salins ◽  
C.S. Godin ◽  
P.P. Lu ◽  
...  

Currently. N-methyl-N'-nitroguanidine (MNG) is being considered by the U.S. Air Force Armament Laboratory for use in explosive formulations. A mammalian toxicity profile has been performed which includes the analysis of chemical impurities and an assessment of the potential for the metabolism of MNG to 1-methyl-3-nitro-1-nitrosoguanidine (MNNG). Potential in situ gastric conversion of MNG to MNNG is a toxicological concern because MNNG is both mutagenic and carcinogenic. The compound was also evaluated in several bioassays to assess its potential genotoxic activity. The acute oral toxicity was determined in male and female Fischer 344 rats administered a single dose of MNG in corn oil. The maximum suspension of MNG that could be delivered, 1 mg MNG/kg body weight, produced no signs of toxic stress during the 14-day observation period. The primary eye and skin irritation potential of MNG was determined in female New Zealand white rabbits using the Draize technique. MNG produced no irritation to intact skin but did produce mild conjunctival irritation. The response of a single guinea pig to the dermal sensitization evaluation indicated that MNG is a weak sensitizer. The results of three genetic tests indicated that MNG does not interact with genetic material. Gastric contents and feces from treated animals showed no evidence of conversion of MNG to MNNG.

2018 ◽  
Vol 12 (26) ◽  
pp. 389-396 ◽  
Author(s):  
Mengiste Berhan ◽  
Dires Kassahun ◽  
Lulekal Ermias ◽  
Arayaselassie Mahlet ◽  
Zenebe Tizazu ◽  
...  

2009 ◽  
Vol 24 (3) ◽  
pp. 221-226 ◽  
Author(s):  
Dragica Brkic ◽  
Slavica Gasic ◽  
Nesko Neskovic

An acute oral toxicity study of the herbicide GAL-57 (Avalon), a mixture of bentazon and dicamba as active ingredients, was investigated on rats, using a new method that has been used in the past several years (2001). Clinical observations symptoms and mortality were performed for all animals in different time intervals after treatment, and gross necropsy was performed at the end of observation period. Clinical symptoms (decreased activity, prone position, abnormal limb position, decreased righting reflex, decreased grip and limb tone, decreased body and abdominal tone, dyspnoea) of marked degree were noted after administration of 2000 mg/kg, and animals were dead in the period of 30-60 minutes after the treatment. GAL-57 did not cause any clinical sings at single 300 mg/kg bw dose. The physical condition and behavior of animals (males and females) were normal, and it is not differ in reaction to the control. According to the methodology used in the present study, it could be concluded that the acute oral LD-50 value of the GAL-57 proved to be between 300 and 2000 mg/kg body weight in rats, and the product was ranked into Poison group III according to Serbian criteria, category 4 of the Global Harmonized Classification System, and Category III of the EPA classification.


2005 ◽  
Vol 24 (3_suppl) ◽  
pp. 65-74

Octyldodecyl Stearoyl stearate is an ester that functions as a skin-conditioning agent and viscosity-increasing agent. It is reported to be used in 105 cosmetic products at concentrations from 2% to 15%. In an isolated human skin permeation and penetration study, 0.005% of the applied dose permeated the skin, around 3% was found in the epidermis, around 1.5% was in tape stripped skin layers, and around 95% stayed in the material applied to the skin. A formulation having 20.6 % Octyldodecyl Stearoyl stearate was classified as minimally to mildly irritating in an in vitro ocular irritation assay. Several tests of products containing from 7.5% to 12.7% Octyldodecyl Stearoyl stearate using rabbits produced minimal to mild ocular irritation. One test of 100% Octyldodecyl Stearoyl stearate (a trade compound) and another of 10% Octyldodecyl Stearoyl stearate in corn oil using rabbits produced no ocular irritation. Tests using rabbits demonstrated that Octyldodecyl Stearoyl stearate at use concentrations was non- to mildly irritating to skin; only one study reported moderate irritation. Octyldodecyl Stearoyl stearate was not mutagenic, with or without S-9 activation, in an Ames test and did not produce a significant increase in micronucleated cells in a mouse in vivo study. In clinical single-insult patch tests at use concentrations, Octyldodecyl Stearoyl stearate was nonirritating to mildly irritating; in a cumulative irritation study, it caused mild irritation. Octyldodecyl Stearoyl stearate was nonsensitizing in clinical tests. Because few toxicity data were available on Octyldodecyl Stearoyl Stearate, summaries of data from existing safety assessments of related ingredients (Octyl Dodecanol, Stearic Acid, and Octyl Stearate) were included. Undiluted Octyl Dodecanol was nontoxic during acute oral and dermal studies using rats and guinea pigs. Stearic Acid was nontoxic to rats during acute oral studies, but caused toxicity during subchronic studies. Rabbits treated topically with the acid were not affected adversely, and mild erythema and slight induration were observed when Stearic Acid was administered intradermally to guinea pigs and rabbits. Octyl stearate had very low acute oral toxicity in rats and mice. Octyl Dodecanol produced only transient mild ocular irritation in rabbits when administered at concentrations up to 100%. Octyl Dodecanol (30% and 100%) was nonirritating to skin in one study using rabbits. In another study using multiple species, 100% Octyl Dodecanol (described as technical grade) caused severe skin irritation in rabbits, moderate irritation in guinea pigs and rats, and no irritation in swine. Stearic Acid was non- to moderately irritating in animal studies, and did not cause photosensitization. In studies using rabbits, undiluted Octyl stearate caused slight, transient ocular irritation, and minimal skin irritation. Stearic Acid did not induce mitotic crossovers and aneuploidy in Saccharomyces cerevisiae, and was nonmutagenic in the Ames test. In a feeding study using mice, Stearic Acid was noncarcinogenic at doses up to 50 g/kg/day. Mice given subcutaneous injections of the acid had low incidences of carcinomas, sarcomas, and lymphomas. In clinical studies, concentrations of up to 100% Octyl Dodecanol were non- to mildly irritating, nonsensitizing, nonphototoxic, and non-photosensitizing. Stearic Acid was nonirritating at concentrations up to 100%, and at concentrations up to 13% it was nonsensitizing and nonphotosensitizing. Octyl stearate (7.6%) in formulation was nonirritating, nonsensitizing, and nonphotosensitizing. Based on skin permeation and penetration data, the Panel does not expect any significant amount of Octyldodecyl Stearoyl stearate to be systemically available. There is no evidence of systemic toxicity associated with any of the related chemicals reviewed in previous safety assessments. None of the available toxicology or clinical data suggest a concern about adverse skin reactions to Octyldodecyl Stearoyl Stearate, or to any of the related chemicals. There is no evidence of ocular toxicity, except for a mild, transient ocular irritation associated with Octyldodecyl Stearoyl stearate and the related chemicals. Overall, Octyldodecyl Stearoyl stearate was considered safe as used in cosmetics.


2008 ◽  
Vol 31 (2) ◽  
pp. 289-301
Author(s):  
Thitinun Monhaphol ◽  
Sirinthorn Yibchok-anun ◽  
Wijit Banlunara ◽  
Mayura Wittayasuporn ◽  
Tanapat Palaga ◽  
...  

1982 ◽  
Vol 1 (4) ◽  
pp. 25-32 ◽  

Polyamino Sugar Condensate (PSC) is the product of a condensation reaction between amino acids and sugars. It appears in over 100 cosmetic preparations at concentrations up to 1%. PSC has an acute oral toxicity greater than 5 g/kg in rats. In tests on rabbits, undiluted PSC was not a primary irritant and produced only mild irritation in some animals. Subacute skin irritation was not observed in rabbits when PSC (undiluted) was applied. Human safety data indicate that PSC is nonsensitizing and, at worst, a mild irritant. PSC is also nonphototoxic. On the basis of the available animal data and limited human experience, it is concluded that Polyamino Sugar Condensate is safe for topical application to humans.


Nano LIFE ◽  
2014 ◽  
Vol 04 (03) ◽  
pp. 1441009 ◽  
Author(s):  
Zhuo Zhao ◽  
Ming Liu ◽  
Xiaochuan Jia ◽  
Hua Wang ◽  
Zhipeng Liu ◽  
...  

Carbon nanotubes (CNT) have been known as one of the most important nanomaterials and their toxicological effects in vivo have been widely concerned. According to "Globally Harmonized System of classification and Labelling of Chemicals" (GHS) classification regulation, here, we analyzed the local toxicity (skin corrosion/irritation), acute oral toxicity, aquatic acute toxicity and reproductive toxicity of single-walled carbon nanotubes (SWCNTs) with the "Organization for Economic Co-operation and Development" (OECD) recommended chemical toxicity standard test methods. The experimental results showed that the LD50 and LC50 of SWCNT are all higher (LC50 more than 5000 mg/kg bw, LC50 more than 100 mg/L), but the skin irritation score is 0.6. As the standard of GHS, that means the SWCNT has no acute oral toxicity and aquatic acute toxicity, but it belongs to skin mild irritation substance. The investigations of reproductive toxicity showed that rate of cell micronuclei formation was significantly increased (p < 0.05) in 10.0 mg/kg dose group, and rate of mice sperm deformity was increased too (p < 0.05) in infected groups indicating that the SWCNT played a potentially role in reproductive toxicity.


1990 ◽  
Vol 1 (2) ◽  
pp. 1-11 ◽  

Glycol Stearate, Glycol Stearate SE, and Glycol Distearate consist primarily of the mono- and diesters of triple-pressed stearic acid. They are used in numerous categories of cosmetic products at concentrations ranging from less than 0.1 to 10%. Animal data for acute oral toxicity, skin and eye irritation, and sensitization show that these ingredients have low acute toxicity. A repeated insult patch test with 50% Glycol Distearate on 125 subjects presented no evidence of skin irritation or hypersensitivity. Human studies using formulations containing Glycol Stearate at levels of 2-5% reported no skin irritation or sensitization. Subchronic testing has not been adequately investigated in laboratory animals. Human test data for formulations containing > 4% Glycol Stearate or Glycol Distearate should be considered. Based on the available information presented herein, it is concluded that Glycol Stearate, Glycol Stearate SE, and Glycol Distearate are safe as cosmetic ingredients in the present practices of use and concentration.


2012 ◽  
Vol 27 (2) ◽  
pp. 188-193 ◽  
Author(s):  
Jung-Ki Kwon ◽  
In-Jung An ◽  
Jin-Seok Lee ◽  
Hae-Ri Kim ◽  
Ha-Seung Park ◽  
...  

1992 ◽  
Vol 11 (1) ◽  
pp. 51-56 ◽  

Isopropyl Linoleate is the ester of isopropyl alcohol and linoleic acid. In cosmetics, it is used as a skin conditioning agent and emollient at concentrations ranging from 0.1 % to 10.0%. In an acute oral toxicity study, none of the albino rabbits that received doses of 10.0% Isopropyl Linoleate in corn oil died. Isopropyl Linoleate (undiluted and 10.0% suspension) were classified as slight ocular irritants. Undiluted Isopropyl Linoleate was classified as a slight skin irritant. The report concludes that the safety of use of Isopropyl Linoleate has not been documented and substantiated, and that it is not possible to conclude that the ingredient is safe for use in cosmetic products. The report details the type of safety test data that is needed to substantiate the safety of use of Isopropyl Linoleate in cosmetic products.


Author(s):  
A. M. Klinkner ◽  
R. A. Weiss ◽  
A. Kelley ◽  
P. J. Bugelski

Polyinosinic:polycytidylic acid is an inducer of interferon and a macrophage activator. We have found that intratracheal instillation of polyI:C (IT-pI:C) activates rat bronchoalveolar lavage cells (BAL) for a variety of functions. Examination of Giemsa stained, cytocentrifuge preparations showed that IT-pI:C induced a population of BAL not seen in resident BAL. The morphology of these cells suggested that they might be derived from blood monocytes. To test this hypothesis we have examined several populations of macrophages that had been stained for endogenous peroxidase activity as a marker of cells derived from the monocyte-macrophage lineage.Macrophages were obtained from Fischer 344 rats. Peritoneal exudate cells (PEC) were collected by lavage 4 days after i.p. injection of 20 ml 3% thioglycolate. Buffy coat monocytes were separated from venous blood from naive rats.


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