TY - JOUR
T1 - Assessing the Benefits of Drug Delivery by Nanocarriers
T2 - A Partico/Pharmacokinetic Framework
AU - Siegel, Ronald A.
AU - Kirtane, Ameya R.
AU - Panyam, Jayanth
N1 - Publisher Copyright:
© 1964-2012 IEEE.
PY - 2017/9
Y1 - 2017/9
N2 - Objective: An in vivo kinetic framework is introduced to analyze and predict the quantitative advantage of using nanocarriers to deliver drugs, especially anticancer agents, compared to administering the same drugs in their free form. Methods: This framework recognizes three levels of kinetics. First is the particokinetics associated with deposition of nanocarriers into tissues associated with drug effect and toxicity, their residence inside those tissues, and elimination of the nanocarriers from the body. Second is the release pattern in time of free drug from the nanocarriers. Third is the pharmacokinetics of free drug, as it relates to deposition and elimination processes in the target and toxicity associated tissues, and total body clearance. A figure of merit, the drug targeting index (DTI), is used to quantitate the benefit of nanocarrier-based drug delivery by considering the effects of preferential deposition of nanoparticles into target tissues and relative avoidance of tissues associated with drug toxicity, compared to drug that is administered in its free form. Results: General methods are derived for calculating DTI when appropriate particokinetic, pharmacokinetic, and drug release rate information is available, and it is shown that relatively simple algebraic forms result when some common assumptions are made. Conclusion: This approach may find use in developing and selecting nanocarrier formulations, either for populations or for individuals.
AB - Objective: An in vivo kinetic framework is introduced to analyze and predict the quantitative advantage of using nanocarriers to deliver drugs, especially anticancer agents, compared to administering the same drugs in their free form. Methods: This framework recognizes three levels of kinetics. First is the particokinetics associated with deposition of nanocarriers into tissues associated with drug effect and toxicity, their residence inside those tissues, and elimination of the nanocarriers from the body. Second is the release pattern in time of free drug from the nanocarriers. Third is the pharmacokinetics of free drug, as it relates to deposition and elimination processes in the target and toxicity associated tissues, and total body clearance. A figure of merit, the drug targeting index (DTI), is used to quantitate the benefit of nanocarrier-based drug delivery by considering the effects of preferential deposition of nanoparticles into target tissues and relative avoidance of tissues associated with drug toxicity, compared to drug that is administered in its free form. Results: General methods are derived for calculating DTI when appropriate particokinetic, pharmacokinetic, and drug release rate information is available, and it is shown that relatively simple algebraic forms result when some common assumptions are made. Conclusion: This approach may find use in developing and selecting nanocarrier formulations, either for populations or for individuals.
KW - Modeling
KW - nanoparticles
KW - targeted drug delivery
UR - https://www.scopus.com/pages/publications/85029856278
UR - https://www.scopus.com/pages/publications/85029856278#tab=citedBy
U2 - 10.1109/TBME.2016.2632733
DO - 10.1109/TBME.2016.2632733
M3 - Article
C2 - 27913319
AN - SCOPUS:85029856278
SN - 0018-9294
VL - 64
SP - 2176
EP - 2185
JO - IEEE Transactions on Biomedical Engineering
JF - IEEE Transactions on Biomedical Engineering
IS - 9
M1 - 7762087
ER -