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1.
J Control Release ; 143(1): 71-9, 2010 Apr 02.
Article in English | MEDLINE | ID: mdl-20043962

ABSTRACT

Endocytic uptake and subcellular trafficking of a large array of HPMA (N-(2-hydroxypropyl)methacrylamide) based copolymers possessing positively or negatively charged residues, or hydrophobic groups were evaluated by flow cytometry and living cell confocal microscopy in cultured prostate cancer cells. The degrees of cellular uptake of various copolymer fractions with narrow polydispersities were quantified. The copolymer charge was the predominant physicochemical feature in terms of cellular uptake. Fast and efficient uptake occurred in positively charged copolymers due to non-specific adsorptive endocytosis, whereas slow uptake of negatively charged copolymers was observed. The uptake of copolymers was also molecular weight dependent. The copolymers were internalized into the cells through multiple endocytic pathways: positively charged copolymers robustly engaged clathrin-mediated endocytosis, macropinocytosis and dynamin-dependent endocytosis, while weakly negatively charged copolymers weakly employed these pathways; strongly negatively charged copolymers only mobilized macropinocytosis. HPMA copolymer possessing 4 mol% of moderately hydrophobic functional groups did not show preferential uptake. All copolymers ultimately localized in late endosomes/lysosomes via early endosomes; with varying kinetics among the copolymers. This study indicates that cell entry and subsequent intracellular trafficking of polymeric drug carriers are strongly dependent on the physicochemical characteristics of the nanocarrier, such as charge and molecular weight.


Subject(s)
Acrylamides/metabolism , Drug Carriers , Endocytosis , Prostatic Neoplasms/metabolism , Acrylamides/chemistry , Biological Transport , Cell Line, Tumor , Chemistry, Pharmaceutical , Chromatography, Gel , Clathrin/metabolism , Endosomes/metabolism , Flow Cytometry , Humans , Hydrophobic and Hydrophilic Interactions , Kinetics , Male , Microscopy, Confocal , Molecular Structure , Molecular Weight , Pinocytosis , Structure-Activity Relationship , Surface Properties , Technology, Pharmaceutical/methods , Transfection , rab GTP-Binding Proteins/genetics , rab GTP-Binding Proteins/metabolism
2.
Biomacromolecules ; 10(7): 1704-14, 2009 Jul 13.
Article in English | MEDLINE | ID: mdl-21197960

ABSTRACT

The basic physicochemical properties that determine the distribution and fate of synthetic macromolecules in living cells were characterized using fluorescently labeled HPMA (N-(2-hydroxypropyl)methacrylamide) copolymers. Twelve different classes of water-soluble copolymers were created by incorporating eight different functionalized comonomers. These comonomers possessed functional groups with positive or negative charges or contained short hydrophobic peptides. The copolymers were fractionated to create parallel "ladders" consisting of 10 fractions of narrow polydispersity with molecular weights ranging from 10 to 200 kDa. The intracellular distributions were characterized for copolymer solutions microinjected into the cytoplasm of cultured ovarian carcinoma cells. Even the highest molecular weight HPMA copolymers were shown to quickly and evenly diffuse throughout the cytoplasm and remain excluded from membrane-bound organelles, regardless of composition. The exceptions were the strongly cationic copolymers, which demonstrated a pronounced localization to microtubules. For all copolymers, nuclear entry was consistent with passive transport through the nuclear pore complex (NPC). Nuclear uptake was shown to be largely dictated by the molecular weight of the copolymers, however, detailed kinetic analyses showed that nuclear import rates were moderately, but significantly, affected by differences in comonomer composition. HPMA copolymers containing amide-terminated phenylalanine-glycine (FG) sequences, analogous to those found in the NPC channel protein, demonstrated a potential to regulate import to the nuclear compartment. Kinetic analyses showed that 15 kDa copolymers containing GGFG, but not those containing GGLFG, peptide pendant groups altered the size-exclusion characteristics of NPC-mediated nuclear import.


Subject(s)
Acrylamides/chemistry , Active Transport, Cell Nucleus , Oligopeptides/chemistry , Ovarian Neoplasms/drug therapy , Polymers/chemical synthesis , Amino Acid Sequence , Cell Line, Tumor , Female , Humans , Hydrophobic and Hydrophilic Interactions , Kinetics , Ovarian Neoplasms/pathology , Polymers/pharmacokinetics
3.
Biomacromolecules ; 7(8): 2347-56, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16903681

ABSTRACT

Semitelechelic HPMA (N-(2-hydroxypropyl)methacrylamide) copolymers possessing a single terminal lipophilic triphenylphosphonium (TPP) cation and fluorescent labels were synthesized to determine how the attached cation affected cellular uptake and intracellular trafficking. In vitro mitochondrial uptake fluorescence quenching assays using isolated mouse liver mitochondria indicated that only lower molecular weight (<5 kDa) BODIPY FL-labeled TPP-semitelechelic HPMA copolymers exhibited significant organelle localization or uptake. In vitro cellular uptake and intracellular trafficking was evaluated using cultured human ovarian carcinoma cells. Cells incubated with all types of TPP copolymers used in the study appeared to internalize the polymer by endocytosis only, and all of the internalized copolymer was confined to the lysosomal compartment after 24 h. Endocytotic uptake of the TPP-HPMA copolymer conjugates was rapid, suggesting that they were internalized by adsorptive endocytosis, rather than fluid-phase pinocytosis. Low-molecular weight (<5 kDa) and high-molecular weight (>5 kDa) semitelechelic copolymers, microinjected into cultured cells indicated that the TPP moiety did not significantly localize the polymers to mitochondria.


Subject(s)
Boron Compounds/chemistry , Endocytosis , Mitochondria , Molecular Probes/chemistry , Organophosphorus Compounds/chemistry , Polymethacrylic Acids/chemistry , Biological Transport , Cell Line, Tumor , Humans , Molecular Probes/chemical synthesis , Molecular Probes/pharmacology , Organophosphorus Compounds/chemical synthesis , Organophosphorus Compounds/pharmacology , Polymethacrylic Acids/chemical synthesis , Polymethacrylic Acids/pharmacology
4.
Bioconjug Chem ; 14(5): 989-96, 2003.
Article in English | MEDLINE | ID: mdl-13129403

ABSTRACT

Specific targeting of ovarian carcinoma cells using pegylated polyethylenimine (PEG-PEI) conjugated to the antigen binding fragment (Fab') of the OV-TL16 antibody, which is directed to the OA3 surface antigen, was the objective of this study. OA3 is expressed by a majority of human ovarian carcinoma cell lines. To demonstrate the ability of the PEG-PEI-Fab' to efficiently complex DNA, an ethidium bromide exclusion assay was performed. Comparison with PEG-PEI or PEI 25 kDa showed only minor differences in the ability to condense DNA. Since conjugation of Fab' to PEG-PEI might influence complex stability, this issue was addressed by incubating the complexes with increasing amounts of heparin. This assay revealed stability similar to that of unmodified PEG-PEI/DNA or PEI 25 kDa/DNA complexes. Complexes displayed a size of approximately 150 nm with a zeta potential close to neutral. The latter property is of particular interest for potential in vivo use, since a neutral surface charge reduces nonspecific interactions. Binding studies using flow cytometry and fluorescently labeled DNA revealed a more than 6-fold higher degree of binding of PEG-PEI-Fab'/DNA complexes to epitope-expressing cell lines compared to unmodified PEG-PEI/DNA complexes. In OA3-expressing OVCAR-3 cells, luciferase reporter gene expression was elevated up to 80-fold compared to PEG-PEI and was even higher than that of PEI 25 kDa. The advantage of this system is its specificity, which was demonstrated by competition experiments with free Fab' in the cell culture media during transfection experiments and by using OA3-negative cells. In the latter case, only a low level of reporter gene expression could be achieved with PEG-PEI-Fab'.


Subject(s)
Genetic Therapy/methods , Immunoglobulin Fab Fragments/metabolism , Ovarian Neoplasms/metabolism , Polyethylene Glycols/pharmacokinetics , Polyethyleneimine/pharmacokinetics , Animals , Cell Line, Tumor , Drug Delivery Systems/methods , Female , Humans , Immunoglobulin Fab Fragments/administration & dosage , Immunoglobulin Fab Fragments/chemistry , Male , Mice , NIH 3T3 Cells , Ovarian Neoplasms/drug therapy , Ovarian Neoplasms/genetics , Polyethylene Glycols/administration & dosage , Polyethylene Glycols/chemistry , Polyethyleneimine/administration & dosage , Polyethyleneimine/chemistry , Salmon
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