Intraperitoneal injection

Over the years animal studies have repeatedly shown that perfluorinated inert fluids are nonirritating to the eyes and skin and practically nontoxic by ingestion, inhalation, or intraperitoneal injection (17,22). Thermal degradation can produce toxic decomposition products including perfluoroisobutene which has a reported LC q of 0.5 ppm (6 hr exposure in rats) (31). This decomposition generally requires temperatures above 200°C. 

This LD q was derived from an intravenous injection and not an intraperitoneal injection. 

Ocular Effects. Pinpoint pupils (miosis) have been observed in individuals following acute exposure to methyl parathion. Electroretinographic changes have been reported in mice following intraperitoneal injection of 1.5 mg of methyl parathion. These changes were a direct effect of methyl parathion on... 

Endosulfan administered by gavage at 1.5 mg/kg/day for 30 days to ovariectomized rats did not influence the relative weights or histology of the uterus, cervix, or vagina compared to ovariectomized control rats that did not receive endosulfan (Raizada et al. 1991). Rats in a positive control group received intraperitoneal injections of estradiol and showed increased relative organ weights and normal development of female reproductive tissues compared to the untreated ovariectomized control rats. 

Catfish (Clarias batrachus) plasma vitellogenin levels were significantly decreased after 48 hours of exposure to 0.0015 mg/L of commercial-grade endosulfan (Chakravorty et al. 1992). Levels did not recover substantially with injections of various hormones, including estradiol. In rainbow trout, endosulfan did not induce vitellogenin production at 9 days after a single intraperitoneal injection of 5 mg/kg in peanut oil (Andersen et al. 1999). 

In this section the intraperitoneal route of liposome administration will be discussed. For a number of diseases this route of administration may be preferred over the intravenous route of administration of liposomes. For example, intraperitoneal injection of drug-... 

Tsilibary and Wissig, 1977 Bettendorf, 1979). Abnormal respiration (as a result of anesthesia) affects the retention time of intraperitoneally injected particles. Anesthesia which stimulates respiration results in a decrease of retention time while respirationsuppressing anesthesia results in the opposite effect (Courtice and Simmonds, 1954). 

In comparison to intravenous administration of MLV, which usually results in a rapid and almost quantitative uptake into liver and spleen, the fraction taken up into these organs is lower after intraperitoneal injection of these large liposomes. The reason might be that liposomes are trapped in lymph nodes and degradation of the liposomes in the peritoneal cavity can occur (Ellens et al., 1981 Parker et al., 1982) besides, several types of liposomes are degraded more quickly in lymphatic fluid than in plasma (Parker et al, 1981a,b). 

Bettendorf, U. (1979). Electronmicroscopic studies on the peritoneal resorption of intraperitoneally injected latex particles via the diaphragmatic lymphatics, Lvmphology. 12. 66-70. 

Mouse Bioassay. The mouse is the traditional animal of choice for detecting biological activity due to STX and TTX. Mice receive an intraperitoneal injection of sample and are observed for symptoms of intoxication, i.e., dypsnea, convulsions, and death. This method is effective for detecting biological activity of STX and TTX in numerous samples. For the standard STX assay, one mouse unit is defined as that quantity of STX injected i.p. in 1 ml solution that will... 

A limited study in animals also presents evidence for increased susceptibility to Streptococcus zooepidomicus (Aran d et al. 1986). Immune system effects observed in mice exposed orally to trichloroethylene included inhibition of cell-mediated immunity, delayed type hypersensitivity, and inhibition of antibody-mediated immunity (Sanders et al. 1982). Female mice appeared to be more sensitive than male mice. A study in which a susceptible strain of mice was treated with intraperitoneal injections of trichloroethylene suggests that trichloroethylene can accelerate the autoimmune response (Khan et al. 1995). The immune system may be a sensitive end point for toxic effects from low-level exposure to trichloroethylene however, no firm conclusions can be drawn from the available information. Additional human and animal studies are needed to better characterize this end point and determine the potential for immunological effects for people exposed to trichloroethylene at hazardous waste sites. 

Next, four male Sprague-Dawley rats were administered NDPA-[2,3- H] by intraperitoneal injection (12). After 12 hours, the animals were sacrificed, and RNA and DNA were isolated from the combined livers by standard procedures. Following addition of unlabeled, authentic 7-propylguanine and 7-isopropylguanine as markers, the nucleic acids were hydrolyzed in perchloric acid at... 

In addition to the well-characterized role of iron in catalysing redox interactions, other metallic contaminants, for example, nickel, may also contribute. In vivo toxicity studies have demonstrated the capacity of nickel particulate compounds to induce tumours following intraperitoneal injection (Pott etal., 1987). Such activity is proportional to their phagocytic uptake, and to the associated respiratory burst and generation of PMN-derived reactive oxygen metabolites (ROMs), a proposed pathogenic mechanism (Evans et al., 1992a). 

Membrane translocating peptides are promising vehicles for the transfer of macromolecules into the tissues. Recent report of Schwarze et al. [249] demonstrated that a signal peptide from Hl-virus could transfer betagalactosidase protein to virtually all tissues in rat after intravenous and intraperitoneal injections. In the case of proteins, folding phenomena affect their membrane translocation and these features may be different for gene-based drugs. 

Renal Effects. Animal studies indicate that degenerative changes in the kidneys may result from acute inhalation exposure to 241 Am. Repeated intraperitoneal injection of241 Am resulted in histopathologic changes in the kidneys of rats. 

Colchicine (a drug used in treatment of gout) and vinblastine (a cancer chemotherapy agent) may decrease liver uptake of americium. In rats that received an intraperitoneal injection of either colchicine and vinblastine prior to an intravenous or intramuscular injection of americium citrate, liver uptake of americium was lower, relative to controls, and kidney and skeletal americium uptake were higher (Seidel 1984, 1985). The effect is thought to involve disruption of hepatic microtubule formation, which is critical to the formation and intracellular processing of lysosomes, the initial site of accumulation of americium in the liver. 

---