Surfactant dysfunction from physical or chemical interactions with endogenous inhibitors during acute pulmonary

ncentrations used correspond to BS-181 chemical information achievable, bioactive and well tolerated concentrations in human serum following treatment with the agents, as indicated by the results of a comprehensive literature search. Adenoviruses The viruses utilized in the experiments are listed in Adenovirus-mediated gene transfer assays Cells were infected for 30 min, washed once, and complete medium was added. After 24 h incubation, luciferase assay was performed. Oncolytic Adenoviruses Main receptor CAR CD46 and unknown avb integrins and CAR CAR CAR avb integrins and CAR avb integrins and CAR CD46 and unknown CAR Ratio{ 5.4 5.0 53 60 67 39 8.5 20 10 Virus Ad5luc1 Ad5/3luc1 Ad5lucRGD Adcox2Mluc AdVEGFluc Ad5-D24RGD RGDCRADcox-2R Ad5/3VEGF-E1 Ad300wt = wild type human Ad5 E1A deleted deleted deleted deleted deleted 24 bp deletion heterologous Cox-2 promoter controlling E1A expression heterologous VEGF promoter controlling E1A expression wild type Reporter luciferase luciferase luciferase luciferase luciferase – Fiber wild type serotype 3 knob RGD motif in HI-loop wild type wild type RGD motif in HI-loop RGD motif in HI-loop serotype 3 knob wild type Ref ATCC CAR = coxsackie-adenovirus receptor. ratio of viral particles to plaque forming units, a quality control measure and indicator of viral packaging efficacy. doi:10.1371/journal.pone.0002917.t001 { The protein concentration was determined using a Bio-Rad DC protein assay kit. Background luciferase activities were subtracted from the readings. In order to analyze the effect of anti-inflammatory reagents on transduction efficacy, Dexamethasone, Sodium Salicylate and Salicylic Acid were added 18 h prior the infection, and the infection and incubation were performed in the presence of the 22803826 substances. These doses did not cause toxicity to cells. In vivo cancer models All animal protocols were reviewed and approved by the Experimental Animal Committee of the University of Helsinki and the Provincial Government of Southern Finland. In efficacy experiment, mice were obtained from Charles River Laboratories and subcutaneous tumors were established by injecting 107 C33A cells into female nu/nu mice. 16109 vp of Ad5luc1, wild-type, Ad5/3VEGF-E1, RGDCRADcox-2R, Ad5D24RGD, or no virus, were injected intratumorally on days 1, 2 and 3. Another group of mice received the virus intravenously as a single injection of 161011 vp on day 1. Tumor size was measured. In the in vivo regulation assay, mice were obtained from Taconic, subcutaneous C33A cell tumors were established as above, and treated with a single intravenous injection of 161011 vp on day 1. To study the effect of a different route of administration, 36108 vp were injected intratumorally on three consecutive days in the RGDCRADcox-2R groups. Mice received intraperitoneal injections of PBS or dexamethasone daily. Tumor size was followed. 5/12 mice receiving intravenous Ad5/3VEGF-E1 treatment died within 12 h. Dexamethasone treatment did not affect toxicity. Livers were harvested and fixed in buffered formalin. Histopathology did not reveal any liver toxicity. Subcutaneous human ovarian cancer tumors were established in female NMRI CD-1 nude, and treated with intratumoral injections of 36108 vp on days 1, 3 and 5. Mice were treated with dexamethasone as above. Regulation of replication by dexamethasone in vivo was analyzed with the Hey cell tumors treated with a single intratumoral injection. Half of the 9874164 mice received dexamethasone. 4 tumors/ group were harvested on da

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