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Absorption respiratory

HEALTH SYMPTOMS inhalation (irritates eyes, nose and throat) skin absorption (respiratory system, narcosis, nausea, loss of consciousness). [Pg.3]

HEALTH SYMPTOMS inhalation (irritation of eyes, skin and nose) skin absorption (respiratory distress, excitement, restlessness, headache, nausea). [Pg.46]

HEALTH SYMPTOMS inhalation (coughing, shortness of breath, build-up of fluid in lungs, wheezing, chest tightness, irritates eyes, skin and respiratory system) skin absorption (respiratory system sensitization, skin sensitization, narcotic effects) contact (destroys tissues of mucous membranes, chemical bums to the skin and eyes, scarring, skin allergies). [Pg.487]

Health and Safety Factors. Animal-feeding studies of DMPPO itself have shown it to be nontoxic on ingestion. The solvents, catalyst, and monomers that are used to prepare the polymers, however, should be handled with caution. Eor example, for the preparation of DMPPO, the amines used as part of the catalyst are flammable toxic on ingestion, absorption, and inhalation and are also severe skin and respiratory irritants (see Amines). Toluene, a solvent for DMPPO, is not a highly toxic material in inhalation testing the TLV (71) is set at 375 mg/m, and the lowest toxic concentration is reported to be 100—200 ppm (72). Toxicity of 2,6-dimethylphenol is typical of alkylphenols (qv), eg, for mice, the acute dermal toxicity is LD q, 4000 mg/kg, whereas the acute oral toxicity is LD q, 980 mg/kg (73). The Noryl blends of DMPPO and polystyrene have PDA approval for reuse food apphcations. [Pg.331]

The actual time required for poly-L-lactide implants to be completely absorbed is relatively long, and depends on polymer purity, processing conditions, implant site, and physical dimensions of the implant. For instance, 50—90 mg samples of radiolabeled poly-DL-lactide implanted in the abdominal walls of rats had an absorption time of 1.5 years with metaboHsm resulting primarily from respiratory excretion (24). In contrast, pure poly-L-lactide bone plates attached to sheep femora showed mechanical deterioration, but Httie evidence of significant mass loss even after four years (25). [Pg.190]

Health and Safety Factors. Neopentanoic acid possesses low toxicity, either by ingestion (oral LD q in rats is 2.0 g/kg) or by skin absorption (dermal LD q in rabbits is 3.16 g/kg). The principal ha2ards associated with neopentanoic acid at ambient temperatures are from eye and skin irritation. At elevated temperatures, where concentrations of the vapor are significant, irritation of the respiratory tract can also occur. Contact with the material should be avoided. [Pg.104]

Hexachlorocyclotriphosphazene (cycHc trimer) is a respiratory irritant. Nausea has also been noted on exposure (10). Intravenous and intraperitoneal toxicity measurements were made on mice. The highest nonlethal dose (LDq) was measured as 20 mg/kg (11). Linear chloropolymer is also beUeved to be toxic (10). Upon organic substitution, the high molecular weight linear polymers have been shown to be inert. Rat implants of eight different polyphosphazene homopolymers indicated low levels of tissue toxicity (12). EZ has been found to be reasonably compatible with blood (13), and has lower hpid absorption than fiuorosihcone. [Pg.526]

Industrial environments expose individuals to a plethora of airborne chemical compounds in the form of vapors, aerosols, or biphasic mixtures of both. These atmospheric contaminants primarily interface with two body surfaces the respiratory tract and the skin. Between these two routes of systemic exposure to airborne chemicals (inhalation and transdermal absorption) the respiratory tract has the larger surface area and a much greater percentage of this surface exposed to the ambient environment. Or dinary work clothing generally restricts skin exposures to the arms, neck, and head, and special protective clothing ensembles further limit or totally eliminate skin exposures, but breathing exposes much of the airway to contaminants. [Pg.195]

Chemicals have to pass through either the skin or mucous membranes lining the respiratory airways and gastrointestinal tract to enter the circulation and reach their site of action. This process is called absorption. Different mechanisms of entry into the body also greatly affect the absorption of a compound. Passive diffusion is the most important transfer mechanism. According to Pick s law, diffusion velocity v depends on the diffusion constant (D), the surface area of the membrane (A), concentration difference across the membrane (Ac), and thickness of the membrane (L)... [Pg.263]

Cocaine. This lias a bitter taste, is mydriatic, produces local anaesthesia and is toxic. After absorption, or when taken internally, it acts chiefly by stimulation of the central nervous system, succeeded by depression. Since the two phases may be present in different areas simultaneously, a mixed result may ensue. With large doses the chief symptoms are those of medullary depression. Death is due to paralysis of the respiratory centre. The main use of cocaine in medicine is as a local anaesthetic. [Pg.106]

PuAEMACoLOGiCAL AcTiox. Curare is stated to be almost inert when taken by mouth, owing to poor absorption by intestinal mucous membrane and the rapidity of elimination. Injected hypodermically it is a rapid and potent poison, paralysing the motor nerve-endings in striped muscle, so that voluntary movements cease and death occurs from respiratory failure. [Pg.390]

Rapid absorption of DNPA causes marked irritation of respiratory tract, skin and eyes DNPA is used as a binder in artillery pro-pints and in conens of 10—15% has a burning... [Pg.322]

When kaolin or aluminum is administered widi die lincosamides, die absorption of the lincosamide is decreased. When the lincosamides are administered with the neuromuscular blocking drag (drag diat are used as adjuncts to anesthetic drag diat cause paralysis of the respiratory system) die action of die neuromuscular blocking drug is enhanced, possibly leading to severe and profound respiratory depression. [Pg.87]


See other pages where Absorption respiratory is mentioned: [Pg.478]    [Pg.12]    [Pg.80]    [Pg.479]    [Pg.77]    [Pg.204]    [Pg.375]    [Pg.227]    [Pg.231]    [Pg.65]    [Pg.227]    [Pg.183]    [Pg.115]    [Pg.11]    [Pg.41]    [Pg.145]    [Pg.261]    [Pg.202]    [Pg.221]    [Pg.367]    [Pg.596]    [Pg.480]    [Pg.144]    [Pg.473]    [Pg.628]    [Pg.97]    [Pg.137]    [Pg.50]   
See also in sourсe #XX -- [ Pg.94 , Pg.95 , Pg.96 ]




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Respiratory Transport and Absorption

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Retention, clearance and absorption in the respiratory tract

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