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1.
Biomacromolecules ; 19(1): 71-84, 2018 01 08.
Artículo en Inglés | MEDLINE | ID: mdl-29227674

RESUMEN

Drug delivery to bone is challenging, whereby drug distribution is commonly <1% of injected dose, despite development of several bone-targeted drug delivery systems specific to hydroxyapatite. These bone-targeted drug delivery systems still suffer from poor target cell localization within bone, as at any given time overall bone volume is far greater than acutely remodeling bone volume, which harbors relevant cell targets (osteoclasts or osteoblasts). Thus, there exists a need to target bone-acting drugs specifically to sites of bone remodeling. To address this need, this study synthesized oligo(ethylene glycol) copolymers based on a peptide with high affinity to tartrate-resistant acid phosphatase (TRAP), an enzyme deposited by osteoclasts during the bone resorption phase of bone remodeling, which provides greater specificity relevant for bone cell drugging. Gradient and random peptide orientations, as well as polymer molecular weights, were investigated. TRAP-targeted, high molecular weight (Mn) random copolymers exhibited superior accumulation in remodeling bone, where fracture accumulation was observed for at least 1 week and accounted for 14% of tissue distribution. Intermediate and low Mn random copolymer accumulation was lower, indicating residence time depends on Mn. High Mn gradient polymers were cleared, with only 2% persisting at fractures after 1 week, suggesting TRAP binding depends on peptide density. Peptide density and Mn are easily modified in this versatile targeting platform, which can be applied to a range of bone drug delivery applications.


Asunto(s)
Sistemas de Liberación de Medicamentos , Péptidos/metabolismo , Polímeros/farmacocinética , Acrilamida/química , Animales , Remodelación Ósea , Células Cultivadas , Femenino , Colorantes Fluorescentes/química , Humanos , Masculino , Ratones Endogámicos C57BL , Peso Molecular , Osteoclastos/enzimología , Péptidos/química , Polímeros/química , Fosfatasa Ácida Tartratorresistente/metabolismo , Distribución Tisular
2.
Biomacromolecules ; 18(12): 4054-4059, 2017 Dec 11.
Artículo en Inglés | MEDLINE | ID: mdl-28968079

RESUMEN

A common issue with hydrogel formulations is batch-to-batch irreproducibility originating from poorly defined polymer precursors. Here, we report the use of dendritic polymer end-groups to address this issue and maintain reproducibility between batches of poly(ethylene glycol) (PEG) hydrogels. Specifically, we synthesized two end-functionalized PEG chains: one with azide-terminated first- and second-generation dendrons and the other with strained cyclooctynes. The two complementary azide and alkyne polymers react via strain-promoted alkyne-azide cycloaddition (SPAAC) to produce hydrogels quickly in the absence of additional reagents or catalyst at low polymer concentrations. Hydrogels made with first-generation dendrons gelled in minutes and exhibited a small degree of swelling when incubated in PBS buffer at 37 °C, whereas hydrogels made from second-generation dendrons gelled in seconds with almost no swelling upon incubation at 37 °C. In both cases, the hydrogels proved reproducible, resulting in identical Young's modulus values from different batches. The hydrogels prepared with second-generation dendrons were seeded with human mesenchymal stem cells and showed high cell viability as well as cell spreading over a two-week time frame. These studies show that the SPAAC hydrogels are noncytotoxic and are capable of supporting cell growth.


Asunto(s)
Alquinos/química , Azidas/química , Reactivos de Enlaces Cruzados/química , Dendrímeros/química , Hidrogeles/química , Polietilenglicoles/química , Catálisis , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Reacción de Cicloadición/métodos , Módulo de Elasticidad , Humanos , Células Madre Mesenquimatosas/efectos de los fármacos , Polímeros/química , Reproducibilidad de los Resultados
3.
Tissue Eng Part A ; 27(3-4): 246-255, 2021 02.
Artículo en Inglés | MEDLINE | ID: mdl-32615861

RESUMEN

Characterizing the release profile for materials-directed local delivery of bioactive molecules and its effect on bone regeneration is an important step to improve our understanding of, and ability to optimize, the bone healing response. This study examined the local delivery of parathyroid hormone (PTH) using a thiol-ene hydrogel embedded in a porous poly(propylene fumarate) (PPF) scaffold for bone regeneration applications. The aim of this study was to characterize the degradation-controlled in vitro release kinetics of PTH from the thiol-ene hydrogels, in vivo hydrogel degradation in a subcutaneous implant model, and bone healing in a rat critical size bone defect. Tethering PTH to the hydrogel matrix eliminated the early timepoint burst release that was observed in previous in vitro work where PTH was free to diffuse out of the matrix. Only 8% of the tethered PTH was released from the hydrogel during the first 2 weeks, but by day 21, 80% of the PTH was released, and complete release was achieved by day 28. In vivo implantation revealed that complete degradation of the hydrogel alone occurred by day 21; however, when incorporated in a three-dimensional printed osteoconductive PPF scaffold, the hydrogel persisted for >56 days. Treatment of bone defects with the composite thiol-ene hydrogel-PPF scaffold, delivering either 3 or 10 µg of tethered PTH 1-84, was found to increase bridging of critical size bone defects, whereas treatment with 30 µg of tethered PTH resulted in less bone ingrowth into the defect area. Continued development of this biomaterial delivery system for PTH could lead to improved therapies for treatment of nonunion fractures and critical size bone defects.


Asunto(s)
Regeneración Ósea , Hormona Paratiroidea , Animales , Materiales Biocompatibles , Hidrogeles , Cinética , Hormona Paratiroidea/farmacología , Ratas
4.
J Orthop Res ; 38(3): 536-544, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-31709588

RESUMEN

Neither allograft nor commercially available bone graft substitutes provide the same quality of bone healing as autograft. Incorporation of bioactive molecules like parathyroid hormone (PTH) within bone graft substitute materials may provide similar, if not better treatment options to grafting. The goal of this work was to develop a biomaterial system for the local delivery of PTH to large bone defects for promoting bone regeneration. PTH was loaded in a thiol-ene hydrogel at several concentrations and polymerized in and around an osteoconductive poly(propylene fumarate) (PPF) scaffold. PTH was shown to be bioactive when released from the hydrogel for up to 21 days. Eighty percent of the PTH was released by day 3 with the remaining 20% released by day 14. Bone healing was quantified in rat critical size femoral defects that were treated with hydrogel/PPF and 0, 1, 3, 10, or 30 µg of PTH. Although complete osseous healing was not observed in all samples in any one treatment group, all samples in the 10 µg PTH group were bridged fully by bone or a combination of bone and cartilage containing hypertrophic chondrocytes and endochondral ossification. Outcome measures indicated improved defect bridging by a combination of bony and cartilaginous tissue in the 10 µg treatment group compared with empty bone defects and defects treated with only hydrogel/PPF (i.e., without PTH). Given the tailorability of the hydrogel, future studies will investigate the effects of prolonged gradual PTH release on bone healing. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 38:536-544, 2020.


Asunto(s)
Enfermedades Óseas/terapia , Regeneración Ósea/efectos de los fármacos , Sistemas de Liberación de Medicamentos , Hidrogeles/química , Hormona Paratiroidea/administración & dosificación , Compuestos de Sulfhidrilo/química , Animales , Materiales Biocompatibles , Sustitutos de Huesos , Huesos/efectos de los fármacos , Condrocitos/citología , Fémur/cirugía , Fumaratos/química , Cinética , Masculino , Osteogénesis/efectos de los fármacos , Polipropilenos/química , Ratas , Ratas Sprague-Dawley , Resultado del Tratamiento , Ursidae , Microtomografía por Rayos X
5.
Biomaterials ; 223: 119430, 2019 12.
Artículo en Inglés | MEDLINE | ID: mdl-31493696

RESUMEN

Cells are capable of sensing the differences in elastic and viscous properties (i.e., the 'viscoelasticity') of their tissue microenvironment and responding accordingly by changing their transcriptional activity and modifying their behaviors. When designing viscoelastic materials to mimic the mechanical properties of native tissue niches, it is important to consider the timescales over which cells probe their microenvironment, as the response of a viscoelastic material to an imposed stress or strain is timescale dependent. Although the timescale of cellular mechano-sensing is currently unknown, hydrogel substrates with tunable viscoelastic spectra can allow one to probe the cellular response to timescale dependent mechanical properties. Here, we report on a cytocompatible and viscoelastic hydrogel culture system with reversible boronate ester cross-links, formed from pendant boronic acid and vicinal diol moieties, where the equilibrium kinetics of esterification were leveraged to tune the viscoelastic spectrum. We found that viscoelasticity increased as a function of the boronic acid and vicinal diol concentration, and also increased with decreasing cross-linker concentration, where the maximal loss tangent achieved with this system was 0.55 at 0.1 rad s-1. Additionally, we found that the cis-vicinal diols configuration altered the viscoelastic spectra, where a tan δ peak occurred at ~1 rad s-1 for hydrogels functionalized with boronic acid, while an additional peak formed at ≥10 rad s-1 for hydrogels functionalized with both boronic acid and cis-vic-diols. In experiments with NIH-3T3 fibroblasts cultured on these hydrogels, the projected cell area and nuclear area, focal adhesion tension, and subcellular localization of YAP/TAZ were all found to be lower for cells cultured on the viscoelastic hydrogels compared to elastic hydrogels with a similar storage modulus. Despite these differences, there was not a statistically significant relationship between the frequency dependent viscoelastic material properties characterized in this study and cellular morphologies, focal adhesion tension, or the subcellular localization of YAP. While these results demonstrate that mechanotransduction pathways are affected by viscoelasticity, they also suggest that these mechanotransduction pathways are not particularly sensitive to the frequency dependent viscoelastic material properties from 0.1 to 10 rad s-1.


Asunto(s)
Materiales Biocompatibles/química , Ácidos Borónicos/química , Ésteres/química , Hidrogeles/química , Mecanotransducción Celular , Proteínas Adaptadoras Transductoras de Señales/metabolismo , Animales , Proteínas de Ciclo Celular/metabolismo , Elasticidad , Transferencia Resonante de Energía de Fluorescencia , Cinética , Ratones , Células 3T3 NIH , Reología , Transactivadores/metabolismo , Viscosidad , Proteínas Señalizadoras YAP
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