Literature DB >> 23795337

COMPARATIVE PHARMACOKINETICS OF PAMAM-OH DENDRIMERS AND HPMA COPOLYMERS IN OVARIAN-TUMOR-BEARING MICE.

S Sadekar1, O Linares, Gj Noh, D Hubbard, A Ray, M Janát-Amsbury, C M Peterson, J Facelli, H Ghandehari.   

Abstract

The purpose of this study was to model data from a head to head comparison of the in vivo fate of hyper-branched PAMAM dendrimers with linear HPMA copolymers in order to understand the influence of molecular weight (MW), hydrodynamic size (Rh) and polymer architecture on biodistribution in tumor-bearing mice using compartmental pharmacokinetic analysis. Plasma concentration data was modeled by two-compartment analysis using Winnonlin® to obtain elimination clearance (E.CL) and plasma exposure (AUCplasma). Renal clearance (CLR) was calculated from urine data collected over 1 week. A plasma-tumor link model was fitted to experimental plasma and tumor data by varying the tumor extravasation (K4, K6) and elimination (K5) rate constants using multivariable constrained optimization solver in Matlab®. Tumor exposures (AUCtumor) were computed from area under the tumor concentration time profile curve by the linear trapezoidal method. Along with MW and Rh, polymer architecture was critical in affecting the blood and tumor pharmacokinetics of the PAMAM-OH dendrimers and HPMA copolymers. Elimination clearance decreased more rapidly with increase in hydrodynamic size for PAMAM-OH dendrimers as compared to HPMA copolymers. HPMA copolymers were eliminated renally to a higher extent than PAMAM-OH dendrimers. These results are suggestive of a difference in extravasation of polymers of varying architecture through the glomerular basement membrane. While the linear HPMA copolymers can potentially reptate through a pore smaller in size than their hydrodynamic radii in a random coil conformation, PAMAM dendrimers have to deform in order to permeate across the pores. With increase in molecular weight or generation, the deforming capacity of PAMAM-OH dendrimers is known to decrease, making it harder for higher generation PAMAM-OH dendrimers to sieve through the glomerulus as compared to HPMA copolymers of comparable molecular weights. PAMAM-OH dendrimer had greater tumor extravsation rate constants and higher tumor to plasma exposure ratios than HPMA copolymers of comparable molecular weights which indicated that in the size range studied, when in circulation, PAMAM-OH dendrimers had a higher affinity to accumulate in the tumor than the HPMA copolymers.

Entities:  

Keywords:  N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer; compartmental pharmacokinetics; poly(amido amine) (PAMAM) dendrimer; polymer architecture

Year:  2013        PMID: 23795337      PMCID: PMC3685189          DOI: 10.1007/s13346-012-0119-6

Source DB:  PubMed          Journal:  Drug Deliv Transl Res        ISSN: 2190-393X            Impact factor:   4.617


  33 in total

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Authors:  A Pluen; P A Netti; R K Jain; D A Berk
Journal:  Biophys J       Date:  1999-07       Impact factor: 4.033

2.  Effects of glomerular filtration rate on Ficoll sieving coefficients (theta) in rats.

Authors:  C Rippe; D Asgeirsson; D Venturoli; A Rippe; B Rippe
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3.  Poly(amidoamine) (PAMAM) dendrimers: from biomimicry to drug delivery and biomedical applications.

Authors:  R Esfand; D A. Tomalia
Journal:  Drug Discov Today       Date:  2001-04-01       Impact factor: 7.851

4.  Macromolecule transport across glomerular capillaries: application of pore theory.

Authors:  W M Deen; M P Bohrer; B M Brenner
Journal:  Kidney Int       Date:  1979-09       Impact factor: 10.612

5.  Dendrimers as multi-purpose nanodevices for oncology drug delivery and diagnostic imaging.

Authors:  D A Tomalia; L A Reyna; S Svenson
Journal:  Biochem Soc Trans       Date:  2007-02       Impact factor: 5.407

Review 6.  Ficoll and dextran vs. globular proteins as probes for testing glomerular permselectivity: effects of molecular size, shape, charge, and deformability.

Authors:  Daniele Venturoli; Bengt Rippe
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Review 7.  Development of HPMA copolymer-anticancer conjugates: clinical experience and lessons learnt.

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8.  A modeling analysis of the effects of molecular size and binding affinity on tumor targeting.

Authors:  Michael M Schmidt; K Dane Wittrup
Journal:  Mol Cancer Ther       Date:  2009-10       Impact factor: 6.261

9.  HPMA copolymers: origins, early developments, present, and future.

Authors:  Jindrich Kopecek; Pavla Kopecková
Journal:  Adv Drug Deliv Rev       Date:  2009-11-14       Impact factor: 15.470

10.  Physiologic upper limit of pore size in the blood-tumor barrier of malignant solid tumors.

Authors:  Hemant Sarin; Ariel S Kanevsky; Haitao Wu; Alioscka A Sousa; Colin M Wilson; Maria A Aronova; Gary L Griffiths; Richard D Leapman; Howard Q Vo
Journal:  J Transl Med       Date:  2009-06-23       Impact factor: 5.531

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  4 in total

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2.  Uniform brain tumor distribution and tumor associated macrophage targeting of systemically administered dendrimers.

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3.  Meta-Analysis of Nanoparticle Delivery to Tumors Using a Physiologically Based Pharmacokinetic Modeling and Simulation Approach.

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4.  The Impact of Polymer Size and Cleavability on the Intravenous Pharmacokinetics of PEG-Based Hyperbranched Polymers in Rats.

Authors:  Nirmal Marasini; Changkui Fu; Nicholas L Fletcher; Christopher Subasic; Gerald Er; Karine Mardon; Kristofer J Thurecht; Andrew K Whittaker; Lisa M Kaminskas
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  4 in total

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