Guilin Qiao

Ding, H. Z., Zeng, Z. L., Fung, K. F., Chen, Z. L., & Qiao, G. L. (2001). Pharmacokinetics of sarafloxacin in pigs and broilers following intravenous, intramuscular, and oral single-dose applications. JOURNAL OF VETERINARY PHARMACOLOGY AND THERAPEUTICS, 24(5), 303–308. https://doi.org/10.1046/j.1365-2885.2001.00348.x

Qiao, G. L., & Riviere, J. E. (2000). Dermal absorption and tissue disposition of 3,3',4,4'-tetrachlorobiphenyl (TCB) in an ex vivo pig model: Assessing the impact of dermal exposure variables. International Journal of Occupational and Environmental Health, 6, 127–137. https://doi.org/10.1179/oeh.2000.6.2.127

Baynes, R. E., Monteiro-Riviere, N. A., Qiao, G. L., & Riviere, J. E. (1997). Cutaneous toxicity of the benzidine dye direct red 28 applied as mechanistically-defined chemical mixtures (MDCM) in perfused porcine skin. Toxicology Letters, 93(2-3), 159–169. https://doi.org/10.1016/S0378-4274(97)00083-0

Qiao, G. L., Brooks, J. D., & Riviere, J. E. (1997). Pentachlorophenol dermal absorption and disposition from soil in swine: Effects of occlusion and skin microorganism inhibition. TOXICOLOGY AND APPLIED PHARMACOLOGY, 147(2), 234–246. https://doi.org/10.1006/taap.1997.8288

Riviere, J. E., Brooks, J. D., Qiao, G. L., & Monteiro-Riviere, N. A. (1997). Percutaneous absorption of volatile chemicals. In (NTIS report AFOSR G49620-95-1-0017) (pp. 1–23). https://doi.org/10.21236/ada332910

Qiao, G. L., Brooks, J. D., Baynes, R. E., MonteiroRiviere, N. A., Williams, P. L., & Riviere, J. E. (1996). The use of mechanistically defined chemical mixtures (MDCM) to assess component effects on the percutaneous absorption and cutaneous disposition of topically exposed chemicals .1. Studies with parathion mixtures in isolated perfused porcine skin. TOXICOLOGY AND APPLIED PHARMACOLOGY, 141(2), 473–486. https://doi.org/10.1006/taap.1996.0313

Williams, P. L., Thompson, D., Qiao, G. L., Monteiro-Riviere, N. A., Baynes, R. L., & Riviere, J. E. (1996). The use of mechanistically defined chemical mixtures (MDCM) to assess mixture component effects on the percutaneous absorption and cutaneous disposition of topically exposed chemicals .2. Development of a general dermatopharmacokinetic model for use in risk assessment. TOXICOLOGY AND APPLIED PHARMACOLOGY, 141(2), 487–496. https://doi.org/10.1006/taap.1996.0314

Qiao, G. L., & Riviere, J. E. (1995). Significant Effects of Application Site and Occlusion on the Pharmacokinetics of Cutaneous Penetration and Biotransformation of Parathion in Vivo in Swine. Journal of Pharmaceutical Sciences, 84(4), 425–432. https://doi.org/10.1002/jps.2600840408

Qiao, G. L., Williams, P. L., & Riviere, J. E. (1994). Percutaneous absorption, biotransformation and systemic disposition of parathion in vivo in swine. I. Comprehensive pharmacokinetic model. Drug Metabolism and Disposition, 22, 459–471.

Qiao, G. L., Chang, S. K., & Riviere, J. E. (1993). Effects of Anatomical Site and Occlusion on the Percutaneous Absorption and Residue Pattern of 2,6-(ring-14C)Parathion in Vivo in Pigs. Toxicology and Applied Pharmacology, 122(1), 131–138. https://doi.org/10.1006/taap.1993.1180