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Toxicokinetics

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189:, and its potential to bioaccumulate. Toxicokinetic profiles can change with increasing exposure duration or dose. Real world environmental exposures generally occur as low level mixtures, such as from air, water, food, or tobacco products. Mixture effects may differ from individual chemical toxicokinetic profiles because of chemical interactions, synergistic, or competitive processes. For other reasons, it is equally important to characterize the toxicokinetics of individual chemicals constituents found in mixtures as information on behavior or fate of the individual chemical can help explain environmental, human, and wildlife biomonitoring studies. 253: 22: 170:, distribution, metabolism and excretion (ADME). Absorption describes the entrance of the chemical into the body, and can occur through the air, water, food, or soil. Once a chemical is inside a body, it can be distributed to other areas of the body through diffusion or other biological processes. At this point, the chemical may undergo metabolism and be biotransformed into other chemicals ( 141:
experiments in animals and the corresponding exposures in humans. However, it can also be used in environmental risk assessments in order to determine the potential effects of releasing chemicals into the environment. In order to quantify toxic effects, toxicokinetics can be combined with
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developed to describe and predict the behavior of a toxicant in an animal body; for example, what parts (compartments) of the body a chemical may tend to enter (e.g. fat, liver, spleen, etc.), and whether or not the chemical is expected to be metabolized or excreted and at what rate.
121:(often abbreviated as 'TK') is the description of both what rate a chemical will enter the body and what occurs to excrete and metabolize the compound once it is in the body. 181:
A well designed toxicokinetic study may involve several different strategies and depends on the scientific question to be answered. Controlled
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occurs, the metabolites may leave the body, be transformed into other compounds, or continue to be stored in the body compartments.
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and repeated toxicokinetic animal studies are useful to identify a chemical's biological persistence, tissue and whole body
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to determine the relationship between the systemic exposure of a compound and its
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toxicodynamics. Such toxicokinetic-toxicodynamic (TKTD) models are used in
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Four potential processes exist for a chemical interacting with an animal:
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Szabo DT, Diliberto JJ, Hakk H, Huwe JK, Birnbaum LS (2010).
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a website on mathematical models in ecotoxicology).
46:. Unsourced material may be challenged and removed. 153:Similarly, physiological toxicokinetic models are 305: 124: 288: 295: 281: 223: 106:Learn how and when to remove this message 306: 247: 155:physiological pharmacokinetic models 44:adding citations to reliable sources 15: 13: 14: 340: 251: 20: 31:needs additional citations for 199: 1: 192: 267:. You can help Knowledge by 161: 125:Relation to Pharmacokinetics 7: 10: 345: 246: 329:Medicinal chemistry stubs 129:It is an application of 212:Toxicological Sciences 225:10.1093/toxsci/kfq183 40:improve this article 314:Medicinal chemistry 261:medicinal chemistry 259:This article about 276: 275: 176:biotransformation 116: 115: 108: 90: 336: 319:Pharmacokinetics 297: 290: 283: 255: 248: 238: 237: 227: 203: 131:pharmacokinetics 111: 104: 100: 97: 91: 89: 55:"Toxicokinetics" 48: 24: 16: 344: 343: 339: 338: 337: 335: 334: 333: 304: 303: 302: 301: 244: 242: 241: 204: 200: 195: 164: 127: 112: 101: 95: 92: 49: 47: 37: 25: 12: 11: 5: 342: 332: 331: 326: 321: 316: 300: 299: 292: 285: 277: 274: 273: 256: 240: 239: 197: 196: 194: 191: 163: 160: 126: 123: 119:Toxicokinetics 114: 113: 28: 26: 19: 9: 6: 4: 3: 2: 341: 330: 327: 325: 322: 320: 317: 315: 312: 311: 309: 298: 293: 291: 286: 284: 279: 278: 272: 270: 266: 262: 257: 254: 250: 249: 245: 235: 231: 226: 221: 218:(2): 282–93. 217: 213: 209: 202: 198: 190: 188: 184: 179: 177: 173: 169: 159: 156: 151: 149: 145: 144:ecotoxicology 140: 136: 132: 122: 120: 110: 107: 99: 96:February 2021 88: 85: 81: 78: 74: 71: 67: 64: 60: 57: –  56: 52: 51:Find sources: 45: 41: 35: 34: 29:This article 27: 23: 18: 17: 269:expanding it 258: 243: 215: 211: 201: 180: 165: 152: 148:ecotoxmodels 128: 118: 117: 102: 93: 83: 76: 69: 62: 50: 38:Please help 33:verification 30: 172:metabolites 324:Toxicology 308:Categories 193:References 168:absorption 139:toxicology 66:newspapers 187:half-life 162:Processes 234:20562218 135:toxicity 80:scholar 232:  82:  75:  68:  61:  53:  263:is a 183:acute 146:(see 87:JSTOR 73:books 265:stub 230:PMID 59:news 220:doi 216:117 42:by 310:: 228:. 214:. 210:. 296:e 289:t 282:v 271:. 236:. 222:: 109:) 103:( 98:) 94:( 84:· 77:· 70:· 63:· 36:.

Index


verification
improve this article
adding citations to reliable sources
"Toxicokinetics"
news
newspapers
books
scholar
JSTOR
Learn how and when to remove this message
pharmacokinetics
toxicity
toxicology
ecotoxicology
ecotoxmodels
physiological pharmacokinetic models
absorption
metabolites
biotransformation
acute
half-life
"Toxicokinetics of the flame retardant hexabromocyclododecane gamma: effect of dose, timing, route, repeated exposure, and metabolism"
doi
10.1093/toxsci/kfq183
PMID
20562218
Stub icon
medicinal chemistry
stub

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