RESUMEN
Hyaluronic acid (HA) is one of the most attractive natural polymers employed in biomaterials with biological applications. This polysaccharide is found in different tissues of the body because it is a natural component of the extracellular matrix; furthermore, it has crucial functions in cell growth, migration, and differentiation. Since its biological characteristics, HA has been utilized for the new biomaterial's development for tissue engineering, such as hydrogels. These hydrophilic macromolecular networks have gained significant attention due to their unique properties, making them potential candidates to be applied in biomedical fields. Different mechanisms to obtain hydrogels have been described. However, the research of new non-toxic methods has been growing in recent years. In this study, we prepared a new hydrogel of HA and polyvinyl alcohol by the cost-effective technique of cross-linking by gamma irradiation. The hydrogel was elaborated for the first time and was characterized by several methods such as Fourier Transform Infrared Spectroscopy, Differential Scanning Calorimetry, Thermogravimetric Analysis, and Scanning Electron Microscopy. Likewise, we evaluated the cytotoxicity of the biomaterial and its influence on cell migration in human fibroblasts. Furthermore, we provide preliminary evidence of the wound closure effect in a cellular wound model. The novel hydrogel offers an increase of HA stability with the potential to expand the useful life of HA in its different medical applications.
Asunto(s)
Materiales Biocompatibles/efectos de la radiación , Rayos gamma , Ácido Hialurónico/efectos de la radiación , Polímeros/efectos de la radiación , Alcohol Polivinílico/efectos de la radiación , Materiales Biocompatibles/síntesis química , Materiales Biocompatibles/farmacología , Movimiento Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Fibroblastos/citología , Fibroblastos/efectos de los fármacos , Humanos , Ácido Hialurónico/síntesis química , Ácido Hialurónico/ultraestructura , Microscopía Electrónica de Rastreo , Modelos Químicos , Estructura Molecular , Polímeros/síntesis química , Polímeros/farmacología , Alcohol Polivinílico/síntesis química , Alcohol Polivinílico/farmacología , Espectroscopía Infrarroja por Transformada de Fourier/métodos , Ingeniería de Tejidos/métodosRESUMEN
The exploitation of effective strategies to develop materials bearing deep tissue focal fluorescence imaging capacity and excellent reactive oxygen species (ROS) generation ability is of great interest to address the high-priority demand of photodynamic therapy (PDT). Therefore, we use a rational strategy to fabricate a two-photon-active metal-organic framework via a click reaction (PCN-58-Ps). Moreover, PCN-58-Ps is capped with hyaluronic acid through coordination to obtain cancer cell-specific targeting properties. As a result, the optimized composite PCN-58-Ps-HA exhibits considerable two-photon activity (upon laser excitation at a wavelength of 910 nm) and excellent light-triggered ROS (1O2 and O2â¢-) generation ability. In summary, the interplay of these two critical factors within the PCN-58-Ps-HA framework gives rise to near-infrared light-activated two-photon PDT for deep tissue cancer imaging and treatment, which has great potential for future clinical applications.
Asunto(s)
Antineoplásicos/farmacología , Estructuras Metalorgánicas/farmacología , Fármacos Fotosensibilizantes/farmacología , Antineoplásicos/síntesis química , Antineoplásicos/efectos de la radiación , Apoptosis/efectos de los fármacos , Benzotiazoles/síntesis química , Benzotiazoles/farmacología , Benzotiazoles/efectos de la radiación , Química Clic , Células HEK293 , Células HeLa , Humanos , Ácido Hialurónico/análogos & derivados , Ácido Hialurónico/farmacología , Ácido Hialurónico/efectos de la radiación , Rayos Infrarrojos , Estructuras Metalorgánicas/síntesis química , Estructuras Metalorgánicas/efectos de la radiación , Fotoquimioterapia , Fotones , Fármacos Fotosensibilizantes/síntesis química , Fármacos Fotosensibilizantes/efectos de la radiación , Especies Reactivas de Oxígeno/metabolismoRESUMEN
Soluble microneedles (MNs) of four different hydrophilic polymers namely sodium carboxymethyl cellulose (CMC), polyvinylpyrrolidone (PVP) K30, PVP K90 and sodium hyaluronate (HU) were fabricated by mold casting technique. When exposed to gamma radiation, a dose of 25 kilogray (kGy) was found to render the microneedle (MN) sterile. However, CMC was found to form MNs with poor mechanical properties, whereas PVP K30 MNs were drastically deformed upon exposure to applied dose as observed in bright field microscopy. Scanning electron microscopy (SEM) revealed that morphology of PVP K90 and HU MNs were not significantly affected at the applied dose. The appearances of characteristic peaks of irradiated MNs of PVP K90 and HU in Fourier-transform infrared spectra suggested structural integrity of the polymers on irradiation. Differential scanning calorimetry (DSC) indicated gamma irradiation failed to alter the glass transition temperature and thus mechanical properties of PVP K90 MNs. However, DSC and Powder X-ray Diffraction (PXRD) conclusively indicated that the degree in crystallinity of HU was substantially reduced on irradiation. In vitro dissolution profiles of sterile PVP K90 and HU MNs were similar to un-irradiated MNs with a similarity factor (f2) of 64 and 54, respectively. In vivo dissolution studies in human subjects indicated that sterile MNs of PVP K90 and HU exhibited dissolution of 78.45 ± 1.09 and 78.57 ± 0.70%, respectively, after 20 min. The studies suggested that PVP K90 and HU could be suitable polymers to fabricate soluble MNs as the structural, morphological, microstructural and dissolution properties remained unaltered post γ sterilization.
Asunto(s)
Sistemas de Liberación de Medicamentos/métodos , Rayos gamma/efectos adversos , Polímeros/efectos de la radiación , Esterilización/métodos , Parche Transdérmico , Rastreo Diferencial de Calorimetría , Carboximetilcelulosa de Sodio/química , Carboximetilcelulosa de Sodio/farmacocinética , Carboximetilcelulosa de Sodio/efectos de la radiación , Liberación de Fármacos/efectos de la radiación , Ácido Hialurónico/química , Ácido Hialurónico/farmacocinética , Ácido Hialurónico/efectos de la radiación , Interacciones Hidrofóbicas e Hidrofílicas/efectos de la radiación , Polímeros/química , Polímeros/farmacocinética , Povidona/análogos & derivados , Povidona/química , Povidona/farmacocinética , Povidona/efectos de la radiación , Solubilidad , Difracción de Rayos XRESUMEN
In this study, we have constructed a binary supramolecular nanoassembly composed of α-cyclodextrin-modified hyaluronic acid and an azobenzene-modified diphenylalanine derivative with a positively charged imidazole group. This nanoassembly can bind with siRNA through electrostatic interactions and efficiently delivered them into cancer cells and inhibited their growth.
Asunto(s)
Técnicas de Transferencia de Gen , Ácido Hialurónico/administración & dosificación , Imidazoles/administración & dosificación , ARN Interferente Pequeño/administración & dosificación , alfa-Ciclodextrinas/administración & dosificación , Células A549 , Proliferación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Gliceraldehído-3-Fosfato Deshidrogenasa (Fosforilante)/genética , Células HEK293 , Humanos , Ácido Hialurónico/química , Ácido Hialurónico/efectos de la radiación , Imidazoles/química , Imidazoles/efectos de la radiación , Luz , ARN Interferente Pequeño/química , ARN Interferente Pequeño/efectos de la radiación , alfa-Ciclodextrinas/química , alfa-Ciclodextrinas/efectos de la radiaciónRESUMEN
AIM: This study determined the optimum gamma irradiation dosage to sterilize sodium hyaluronate (HY), single-walled carbon nanotubes (SWCNT), multi-walled carbon nanotubes (MWCNT) and CNT functionalized with HY (HY-SWCNT and HY-MWCNT), evaluated the structural integrity of the materials and assessed whether sterilized materials kept biological properties without affecting renal function. MAIN METHODS: Materials were submitted to dosages of 100 gγ to 30 Kgγ and plated onto agar mediums for colony forming units (CFUs) counting. Sterilized samples were inoculated with 107Bacillus clausii, submitted again to gamma irradiation, and plated in agar mediums for CFUs counting. Scanning electron microscope was used for structural evaluation of sterilized materials. Tooth sockets of rats were treated with sterilized materials for bone formation assessment and renal function of the animals was analyzed. KEY FINDINGS: The optimum gamma dosage for sterilization was 250 gγ for HY and 2.5 Kgγ for the other materials without meaningful structural changes. Sterilized materials significantly increased bone formation (p < 0.05) and they did not compromise renal function and structure. SIGNIFICANCE: Gamma irradiation efficiently sterilized HY, SWCNT, MWCNT, HY-SWCNT and HY-MWCNT without affecting structural aspects while maintaining their desirable biological properties.
Asunto(s)
Materiales Dentales/efectos de la radiación , Rayos gamma , Ácido Hialurónico/efectos de la radiación , Nanotubos de Carbono/efectos de la radiación , Osteogénesis/efectos de los fármacos , Alveolo Dental/efectos de los fármacos , Animales , Bacillus clausii/efectos de la radiación , Recuento de Colonia Microbiana , Materiales Dentales/química , Materiales Dentales/farmacología , Humanos , Ácido Hialurónico/química , Ácido Hialurónico/farmacología , Pruebas de Función Renal , Masculino , Diente Molar/cirugía , Nanotubos de Carbono/química , Nanotubos de Carbono/ultraestructura , Ratas , Ratas Wistar , Esterilización/métodos , Extracción Dental/métodos , Alveolo Dental/microbiología , Alveolo Dental/fisiología , Alveolo Dental/cirugía , Cicatrización de Heridas/efectos de los fármacosRESUMEN
In this study, an injectable and near-infrared (NIR) light-triggered ROS-degradable hyaluronic acid hydrogel platform was developed as localized delivery vehicle for photosensitizer protophorphyrin IX (PpIX) and anticancer drug doxorubicin (DOX), to achieve superior combined chemo-photodynamic therapy with light-tunable on-demand drug release. The in situ-forming hydrogel fabricated readily via the formation of dynamic covalent acylhydrazone bonds could efficiently prevent severe self-quenching effect of water-insoluble PpIX due to the covalent binding, leading to localized enhanced photodynamic therapy (PDT). Moreover, the extensive ROS generated by the hydrogel under NIR light irradiation could not only realize efficient PDT effect, but also cleave the ROS-cleavable small molecule crosslinker, inducing the desirable degradation of hydrogel and subsequent on-demand DOX release for cascaded chemotherapy. The developed versatile hyaluronic acid hydrogels have tunable properties, excellent biocompatibility, biodegradability and exhibit outstanding therapeutic effects in both in vitro cellular experiments and in vivo antitumor studies.
Asunto(s)
Antineoplásicos/administración & dosificación , Doxorrubicina/administración & dosificación , Ácido Hialurónico/administración & dosificación , Hidrogeles/administración & dosificación , Neoplasias/tratamiento farmacológico , Fármacos Fotosensibilizantes/administración & dosificación , Protoporfirinas/administración & dosificación , Animales , Línea Celular , Supervivencia Celular/efectos de los fármacos , Sistemas de Liberación de Medicamentos , Liberación de Fármacos , Femenino , Humanos , Ácido Hialurónico/efectos de la radiación , Rayos Infrarrojos , Ratones Endogámicos BALB C , Fotoquimioterapia , Fármacos Fotosensibilizantes/efectos de la radiación , Protoporfirinas/efectos de la radiaciónRESUMEN
Hyaluronic acid (HA)-based nanocarriers are of great interest in the drug delivery field due to the tumor targetability via CD44-mediated recognition and endocytosis. However, sufficient tumor-specific release of encapsulated cargoes with steady controllability is necessary to optimize their outcome for cancer therapy. In this study, we constructed a light-activated nanocarrier TKHCENPDOX to enable on-demand drug release at the desired site (tumor). Particularly, TKHCENPDOX encapsulating doxorubicin (DOX) was self-assembled from a HA-photosensitizer conjugate (HA-TK-Ce6) containing reactive oxygen species (ROS)-sensitive thioketal (TK) linkers. Following i.v. injection, TKHCENPDOX was accumulated in the MDA-MB-231 breast tumor xenograft more efficiently through preventing drug leakage in the bloodstream and the HA-mediated targeting effect. Upon internalization into tumoral cells, 660 nm laser irradiation generated ROS during a photodynamic (PDT) process to cleave the TK linker next to Ce6, resulting in light-induced TKHCENPDOX dissociation and selective DOX release in the tumor area. Consequently, TKHCENPDOX showed a remarkable therapeutic effect and minimized toxicity in vivo. This strategy might provide new insight for designing cancer-selective nanoplatforms with active targeting and locoregional drug release simultaneously.
Asunto(s)
Antineoplásicos/uso terapéutico , Neoplasias de la Mama/tratamiento farmacológico , Doxorrubicina/uso terapéutico , Portadores de Fármacos/química , Ácido Hialurónico/química , Nanoconjugados/química , Animales , Antineoplásicos/farmacocinética , Línea Celular Tumoral , Clorofilidas , Doxorrubicina/farmacocinética , Portadores de Fármacos/efectos de la radiación , Portadores de Fármacos/toxicidad , Liberación de Fármacos/efectos de la radiación , Femenino , Humanos , Ácido Hialurónico/efectos de la radiación , Ácido Hialurónico/toxicidad , Luz , Ratones Endogámicos BALB C , Ratones Endogámicos ICR , Nanoconjugados/efectos de la radiación , Nanoconjugados/toxicidad , Nanopartículas/química , Nanopartículas/efectos de la radiación , Nanopartículas/toxicidad , Fotoquimioterapia/métodos , Fármacos Fotosensibilizantes/farmacología , Fármacos Fotosensibilizantes/efectos de la radiación , Fármacos Fotosensibilizantes/toxicidad , Porfirinas/farmacología , Porfirinas/efectos de la radiación , Porfirinas/toxicidad , Especies Reactivas de Oxígeno/metabolismo , Ensayos Antitumor por Modelo de XenoinjertoRESUMEN
Skin is constantly exposed to UVR, the most critical risk factor for melanoma development. Hyaluronan is abundant in the epidermal extracellular matrix and may undergo degradation by UVR. It is hypothesized that an intact hyaluronan coat around the cells protects against various agents including UVR, whereas hyaluronan fragments promote inflammation and tumorigenesis. We investigated whether hyaluronan contributes to the UVB-induced inflammatory responses in primary melanocytes. A single dose of UVB suppressed hyaluronan secretion and the expression of hyaluronan synthases HAS2 and HAS3, the hyaluronan receptor CD44, and the hyaluronidase HYAL2, as well as induced the expression of inflammatory mediators IL6, IL8, CXCL1, and CXCL10. Silencing HAS2 and CD44 partly inhibited the inflammatory response, suggesting that hyaluronan coat is involved in the process. UVB alone caused little changes in the coat, but its removal with hyaluronidase during the recovery from UVB exposure dramatically enhanced the surge of these inflammatory mediators via TLR4, p38, and NF-κB. Interestingly, exogenous hyaluronan fragments did not reproduce the inflammatory effects of hyaluronidase. We hypothesize that the hyaluronan coat on melanocytes is a sensor of tissue injury. Combined with UVB exposure, repeated injuries to the hyaluronan coat could maintain a sustained inflammatory state associated with melanomagenesis.
Asunto(s)
Epidermis/efectos de la radiación , Ácido Hialurónico/efectos de la radiación , Melanocitos/inmunología , Transducción de Señal/efectos de la radiación , Rayos Ultravioleta/efectos adversos , Carcinogénesis/inmunología , Carcinogénesis/efectos de la radiación , Células Cultivadas , Quimiocina CXCL1/metabolismo , Quimiocina CXCL10/metabolismo , Epidermis/inmunología , Epidermis/metabolismo , Matriz Extracelular/inmunología , Matriz Extracelular/metabolismo , Matriz Extracelular/efectos de la radiación , Humanos , Receptores de Hialuranos/genética , Receptores de Hialuranos/metabolismo , Hialuronano Sintasas/genética , Hialuronano Sintasas/metabolismo , Ácido Hialurónico/metabolismo , Interleucina-6/metabolismo , Interleucina-8/metabolismo , Melanocitos/metabolismo , Melanocitos/efectos de la radiación , Melanoma/etiología , Melanoma/patología , Cultivo Primario de Células , Transducción de Señal/inmunología , Neoplasias Cutáneas/etiología , Neoplasias Cutáneas/patología , Receptor Toll-Like 4/metabolismoRESUMEN
This study has developed a versatile nano-system with the combined advantages of photothermal effect, active tumor-targeting, temperature-sensitive drug release, and photoacoustic imaging. The nano-system consists of the core of the phase change material (PCM), the outer polypyrrole (PPY) shell and the hyaluronic acid (HA) modified in the PPY shell. The obtained composite nanoparticles (denoted as DTX/PPN@PPY@HA) were spherical with a mean diameter of about 232.7 nm. In vivo and in vitro photoacoustic imaging experiments show that DTX/PPN@PPY@HA is an effective photoacoustic contrast agent, which can be used for accurate localization of tumor region and real-time guidance of photothermal chemotherapy. DTX/PPN@PPY@HA shows good photothermal effects and temperature-sensitive drug release. In addition, cellular experiments showed that DTX/PPN@PPY@HA could be efficiently internalized into tumor cells and produce significant cytotoxicity with the help of near-infrared (NIR) laser. Furthermore, the remarkable inhibition of DTX/PPN@PPY@HA against tumor growth was achieved in 4T1 tumor-bearing mice model.
Asunto(s)
Antineoplásicos/farmacología , Medios de Contraste/química , Docetaxel/farmacología , Portadores de Fármacos/química , Ácido Hialurónico/química , Nanopartículas/química , Animales , Antineoplásicos/administración & dosificación , Neoplasias de la Mama/diagnóstico por imagen , Neoplasias de la Mama/tratamiento farmacológico , Neoplasias de la Mama/patología , Línea Celular Tumoral , Medios de Contraste/administración & dosificación , Medios de Contraste/efectos de la radiación , Medios de Contraste/toxicidad , Docetaxel/administración & dosificación , Portadores de Fármacos/administración & dosificación , Portadores de Fármacos/efectos de la radiación , Portadores de Fármacos/toxicidad , Liberación de Fármacos , Femenino , Colorantes Fluorescentes/química , Humanos , Ácido Hialurónico/administración & dosificación , Ácido Hialurónico/efectos de la radiación , Ácido Hialurónico/toxicidad , Rayos Infrarrojos , Inyecciones Intravenosas , Pulmón/patología , Neoplasias Pulmonares/prevención & control , Neoplasias Pulmonares/secundario , Ratones Endogámicos BALB C , Nanopartículas/administración & dosificación , Nanopartículas/efectos de la radiación , Nanopartículas/toxicidad , Tamaño de la Partícula , Fosfolípidos/administración & dosificación , Fosfolípidos/química , Fosfolípidos/efectos de la radiación , Fosfolípidos/toxicidad , Técnicas Fotoacústicas/métodos , Polímeros/administración & dosificación , Polímeros/química , Polímeros/efectos de la radiación , Polímeros/toxicidad , Pirroles/administración & dosificación , Pirroles/química , Pirroles/efectos de la radiación , Pirroles/toxicidad , Temperatura , Nanomedicina Teranóstica/métodosRESUMEN
In this paper, a novel photo-controlled drug-loaded nanomicelles were self-assembled by the amphiphile of hyaluronan-o-nitrobenzyl-stearyl chain (HA-NB-SC) with doxorubicin (DOX) encapsulated within the hydrophobic core. DOX-loaded HA-NB-SC nanomicelles are â¼139 nm in diameter. CD44-overexpressed HeLa cells can easily take up HA-NB-SC micelles through recognition of HA moiety. DOX-loaded HA-NB-SC nanomicelles could be disassembled upon UV light (365 nm) and consequently, release DOX at desired pathological sites. Furtherly, nitrosobenzaldehyde derivative, photo-induced products of HA-NB-SC and DOX could inhibit the proliferation of HeLa cells together. This strategy may shed some light on delivery of hydrophobic anti-cancer drugs in a controlled manner.
Asunto(s)
Antineoplásicos/farmacología , Doxorrubicina/farmacología , Portadores de Fármacos/química , Ácido Hialurónico/análogos & derivados , Nanoestructuras/química , Tensoactivos/química , Antineoplásicos/química , Doxorrubicina/química , Portadores de Fármacos/síntesis química , Portadores de Fármacos/efectos de la radiación , Portadores de Fármacos/toxicidad , Liberación de Fármacos , Células HEK293 , Células HeLa , Humanos , Ácido Hialurónico/síntesis química , Ácido Hialurónico/efectos de la radiación , Ácido Hialurónico/toxicidad , Luz , Micelas , Nanoestructuras/efectos de la radiación , Nanoestructuras/toxicidad , Nitrobenzoatos/síntesis química , Nitrobenzoatos/química , Nitrobenzoatos/efectos de la radiación , Nitrobenzoatos/toxicidad , Tamaño de la Partícula , Tensoactivos/síntesis química , Tensoactivos/efectos de la radiación , Tensoactivos/toxicidadRESUMEN
Herein, we report novel hyaluronic acid formulated nanoparticles containing a platinum(II) conjugated silicon(IV) phthalocyanine (SiPc-Pt-HA) for tumor targeted red light photodynamic therapy and chemotherapy. The SiPc-Pt-HA conjugate showed specific uptake, photo-enhanced cytotoxicity (~1500 fold) and mitochondrial accumulation in breast cancer over normal cells.
Asunto(s)
Antineoplásicos/farmacología , Ácido Hialurónico/química , Indoles/farmacología , Mitocondrias/metabolismo , Nanopartículas/química , Fármacos Fotosensibilizantes/farmacología , Antineoplásicos/química , Antineoplásicos/efectos de la radiación , Apoptosis/efectos de los fármacos , Línea Celular Tumoral , Células HEK293 , Humanos , Receptores de Hialuranos/metabolismo , Ácido Hialurónico/efectos de la radiación , Indoles/química , Indoles/efectos de la radiación , Isoindoles , Luz , Nanopartículas/efectos de la radiación , Fotoquimioterapia/métodos , Fármacos Fotosensibilizantes/química , Fármacos Fotosensibilizantes/efectos de la radiación , Platino (Metal)/química , Silicio/químicaRESUMEN
The purpose of this study is to conduct modeling and simulation to understand the effect of shock-induced mechanical loading, in the form of cavitation bubble collapse, on damage to the brain's perineuronal nets (PNNs). It is known that high-energy implosion due to cavitation collapse is responsible for corrosion or surface damage in many mechanical devices. In this case, cavitation refers to the bubble created by pressure drop. The presence of a similar damage mechanism in biophysical systems has long being suspected but not well-explored. In this paper, we use reactive molecular dynamics (MD) to simulate the scenario of a shock wave induced cavitation collapse within the perineuronal net (PNN), which is the near-neuron domain of a brain's extracellular matrix (ECM). Our model is focused on the damage in hyaluronan (HA), which is the main structural component of PNN. We have investigated the roles of cavitation bubble location, shockwave intensity and the size of a cavitation bubble on the structural evolution of PNN. Simulation results show that the localized supersonic water hammer created by an asymmetrical bubble collapse may break the hyaluronan. As such, the current study advances current knowledge and understanding of the connection between PNN damage and neurodegenerative disorders.
Asunto(s)
Matriz Extracelular/efectos de la radiación , Ondas de Choque de Alta Energía , Ácido Hialurónico/efectos de la radiación , Simulación de Dinámica Molecular , Neuronas/efectos de la radiación , Estrés MecánicoRESUMEN
Current meniscus tissue repairing strategies involve partial or total meniscectomy, followed by allograft transplantation or synthetic material implantation. However, allografts and synthetic implants have major drawbacks such as the limited supply of grafts and lack of integration into host tissue, respectively. In this study, we investigated the effects of conditioned medium (CM) from meniscal fibrochondrocytes and TGF-ß3 on tonsil-derived mesenchymal stem cells (T-MSCs) for meniscus tissue engineering. CM-expanded T-MSCs were encapsulated in riboflavin-induced photocrosslinked collagen-hyaluronic acid (COL-RF-HA) hydrogels and cultured in chondrogenic medium containing TGF-ß3. In vitro results indicate that CM-expanded cells followed by TGF-ß3 exposure stimulated the expression of fibrocartilage-related genes (COL2, SOX9, ACAN, COL1) and production of extracellular matrix components. Histological assessment of in vitro and subcutaneously implanted in vivo constructs demonstrated that CM-expanded cells followed by TGF-ß3 exposure resulted in highest cell proliferation, GAG accumulation, and collagen deposition. Furthermore, when implanted into meniscus defect model, CM treatment amplified the potential of TGF-ß3 and induced complete regeneration. STATEMENT OF SIGNIFICANCE: Conditioned medium derived from chondrocytes have been reported to effectively prime mesenchymal stem cells toward chondrogenic lineage. Type I collagen is the main component of meniscus extracellular matrix and hyaluronic acid is known to promote meniscus regeneration. In this manuscript, we investigated the effects of conditioned medium (CM) and transforming growth factor-ß3 (TGF-ß3) on tonsil-derived mesenchymal stem cells (T-MSCs) encapsulated in riboflavin-induced photocrosslinked collagen-hyaluronic acid (COL-RF-HA) hydrogel. We employed a novel source of conditioned medium, derived from meniscal fibrochondrocytes. Our in vitro and in vivo results collectively illustrate that CM-expanded cells followed by TGF-ß3 exposure have the best potential for meniscus regeneration. This manuscript highlights a novel stem cell commitment strategy combined with biomaterials designs for meniscus regeneration.
Asunto(s)
Condrocitos/trasplante , Hidrogeles/química , Trasplante de Células Madre Mesenquimatosas/instrumentación , Lesiones de Menisco Tibial/patología , Lesiones de Menisco Tibial/terapia , Andamios del Tejido , Factor de Crecimiento Transformador beta3/administración & dosificación , Animales , Condrocitos/citología , Condrocitos/efectos de los fármacos , Preparaciones de Acción Retardada/administración & dosificación , Preparaciones de Acción Retardada/efectos de la radiación , Diseño de Equipo , Ácido Hialurónico/química , Ácido Hialurónico/efectos de la radiación , Hidrogeles/efectos de la radiación , Luz , Trasplante de Células Madre Mesenquimatosas/métodos , Tonsila Palatina/citología , Fármacos Fotosensibilizantes/química , Fármacos Fotosensibilizantes/efectos de la radiación , Conejos , Riboflavina/química , Riboflavina/efectos de la radiación , Resultado del TratamientoRESUMEN
Current studies have revealed the excellent moisture absorption-retention capacity of hyaluronan (HA); however, HA is easily degraded by hyaluronidase on the surface of skin. So, it is very necessary to develop an alternative derivative with low cytotoxicity and resistance to hyaluronidase. Herein, a HA decorated with photocaged groups was synthesized. The moisture absorption-retention capacity and hyaluronidase resistance of photocaged HA (HA-DMNB) and products of HA-DMNB irradiated by ultraviolet for different time (IHA-DMNB), were investigated. Results show that HA-DMNB is more resistant to hyaluronidase than HA, and HA-DMNB could release free carboxyl groups of HA upon ultraviolet to bond with H2O. More importantly, HA-DMNB was protective against UV light. In addition, HA-DMNB and IHA-DMNB were observed to be nontoxic to HaCat cells. This study indicates that HA-DMNB may be effectively used as a moisture-preserving reagent.
Asunto(s)
Ácido Hialurónico/química , Ácido Hialurónico/efectos de la radiación , Hialuronoglucosaminidasa/metabolismo , Línea Celular , Humanos , Indicadores y Reactivos , Piel , Rayos UltravioletaRESUMEN
Carboxyl group modified zinc phthalocyanines (ZnPc) are classic and widely used photosensitizers (PSs) in upconversion nanoparticles (UCNPs) mediated photodynamic therapy (PDT) for tumor treatment. To improve the PDT activity of the complex system of ZnPc and UCNPs, many UCNPs with high red emission intensity were design and prepared. ZnPc-(COOH)4 tends to aggregate both in water and under physiological conditions, which can sharply decrease its PDT activity. Therefore, choosing monomeric COOH groups modified ZnPc as PSs is an alternative way to improve their activity. In this manuscript, three zinc(ii) phthalocyanines, substituted with 4 (ZnPc-(COOH)4), 8 (ZnPc-(COOH)8) and 16 (ZnPc-(COOH)16) COOH groups, were synthesized. A comparison of the results indicated that ZnPc-(COOH)16 existed in its monomeric form under physiological conditions because of its large substituents. Moreover, ZnPc-(COOH)16 showed superior singlet oxygen (1O2) generation ability when compared to ZnPc-(COOH)4 and ZnPc-(COOH)8. Therefore, we chose ZnPc-(COOH)16 as PSs for absorption on the surface of the UCNPs. Then, they were encapsulated by crosslinked methacrylated hyaluronic acid (m-HA), which provides active tumor accumulation ability by binding its overexpressed receptors on the surface of cancer cells. The resulting nanoparticles can be effectively taken up by cancer cells and shows strong near-infrared (NIR) light triggered PDT in vitro.
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Ácido Hialurónico , Indoles , Nanopartículas , Compuestos Organometálicos , Fotoquimioterapia , Fármacos Fotosensibilizantes , Transporte Biológico , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Geles/química , Geles/efectos de la radiación , Humanos , Ácido Hialurónico/química , Ácido Hialurónico/efectos de la radiación , Indoles/química , Indoles/farmacología , Indoles/efectos de la radiación , Isoindoles , Luz , Nanopartículas/química , Nanopartículas/efectos de la radiación , Compuestos Organometálicos/química , Compuestos Organometálicos/farmacología , Compuestos Organometálicos/efectos de la radiación , Fármacos Fotosensibilizantes/química , Fármacos Fotosensibilizantes/farmacología , Fármacos Fotosensibilizantes/efectos de la radiación , Propano/análogos & derivados , Propano/química , Oxígeno Singlete/metabolismo , Compuestos de ZincRESUMEN
This study focuses on the development of novel biocompatible macroporous cryogels by electron-beam assisted free-radical crosslinking reaction of polymerizable dextran and hyaluronan derivatives. As a main advantage this straightforward approach provides highly pure materials of high porosity without using additional crosslinkers or initiators. The cryogels were characterized with regard to their morphology and their basic properties including thermal and mechanical characteristics, and swellability. It was found that the applied irradiation dose and the chemical composition strongly influence the material properties of the resulting cryogels. Preliminary cytotoxicity tests illustrate the excellent in vitro-cytocompatibility of the fabricated cryogels making them especially attractive as matrices in tissue regeneration procedures.
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Materiales Biocompatibles/síntesis química , Criogeles/síntesis química , Criogeles/toxicidad , Dextranos/química , Dextranos/toxicidad , Ácido Hialurónico/química , Ácido Hialurónico/toxicidad , Células 3T3 , Animales , Materiales Biocompatibles/toxicidad , Supervivencia Celular/efectos de los fármacos , Dextranos/efectos de la radiación , Módulo de Elasticidad , Electrones , Dureza , Ácido Hialurónico/efectos de la radiación , Ensayo de Materiales , Ratones , Conductividad TérmicaRESUMEN
PURPOSE: To analyze the release kinetics and the clinical and histological effects of UV-cross-linked hyaluronic acid as a release-system for the transforming growth factor ß-2 antagonist tranilast with anti-phlogistic properties on intraocular pressure after trabeculectomy in an aggressive scarring animal model. METHODS: Hyaluronate acid was UV-cross linked and loaded with tranilast. The release of tranilast into a buffered salt solution was assessed spectrophotometrically. Glaucoma filtration surgery, similar to that performed in clinical practice, was performed on chinchilla rabbits. The rabbits were divided in 3 groups. (Group A: trabeculectomy alone, group B: trabeculectomy with a cross-linked hyaluronic acid gel preparation and group C: trabeculectomy with cross-linked hyaluronic gel preparation mixed with tranilast). Antifibrotic efficacy was established by clinical response and histologic examination. RESULTS: The cross-linked gels released tranilast for up to 26 h. The release plotted as a function of the square root of time was consistent with a largely diffusion-controlled release system. Both the gel preparation alone and the gel preparation mixed with tranilast were well tolerated in vivo. No adverse effects such as inflammation, corneal toxicity or blurring of the optical media were observed. The intraocular pressure reached preoperative levels within 9 days after surgery in control animals and group B, but remained significantly reduced (p = 0.00016) in the group with tranilast until day 22. CONCLUSIONS: The data of this pilot study suggest that the intraoperative application of UV-crossed linked hyaluronic acid used as a slow release system for tranilast may improve the surgical outcome of glaucoma filtration surgery.
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Antiinflamatorios no Esteroideos/toxicidad , Reactivos de Enlaces Cruzados/química , Sistemas de Liberación de Medicamentos , Ácido Hialurónico/efectos de la radiación , Trabeculectomía , Viscosuplementos/efectos de la radiación , ortoaminobenzoatos/toxicidad , Animales , Antiinflamatorios no Esteroideos/administración & dosificación , Antiinflamatorios no Esteroideos/farmacocinética , Materiales Biocompatibles , Proliferación Celular/efectos de los fármacos , Fibrosis/prevención & control , Glaucoma/cirugía , Proyectos Piloto , Conejos , Rayos Ultravioleta , ortoaminobenzoatos/administración & dosificación , ortoaminobenzoatos/farmacocinéticaRESUMEN
Gold nanoparticles (AuNPs) with diameter from 4 to 10nm, capping by hyaluronan (HA) were synthesized using a γ-irradiation method. The maximum absorption wavelengths at 517-525 nm of colloidal AuNPs/HA solutions were measured by UV-vis spectroscopy. The size and size distribution of AuNPs were determined from TEM images. The influence of various factors on the size of AuNPs particularly the concentration of Au3+ and HA, and dose rate were also investigated. Results indicated that higher dose rate and HA concentration favor smaller sizes of AuNPs whereas the size increases with Au3+ concentration. The colloidal AuNPs/HA solution was fairly stable more than 6 months under storage at ambient condition. The AuNPs stabilized by biocompatible HA with the size less than 10nm as prepared can potentially be applied in biomedicines and cosmetics.
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Rayos gamma , Oro/efectos de la radiación , Ácido Hialurónico/efectos de la radiación , Nanopartículas del Metal/efectos de la radiación , Oro/química , Ácido Hialurónico/química , Nanopartículas del Metal/químicaRESUMEN
Hydrogels are three-dimensional water-insoluble hydrophilic natural or synthetic polymer networks made up of crosslinked water-soluble polymers. The purpose of this study was to develop and directly compare photo crosslinked hydrogels on the basis of pure gelatin, alginate and hyaluronic acid as well as their blends. The functionalization of starting materials with methacrylate moieties was evaluated by 1H-NMR spectroscopy. Hydrogels were prepared from methacrylates by photo cross-linking using UV light. The effect of changing the hydrogel composition was quantified through examination of hydrogel swelling behavior and rheological properties. In addition, the viability and adhesion of neonatal rat cardiomyocytes (NRCM) seeded onto the hydrogels was examined by in vivo imaging of NRCM-mediated scaffold contraction as well as by histological evaluation after immunostaining. Biological testing showed good biocompatibility and cell survival in the presence of all materials discussed. Adhesion of cells could only be observed in the presence of gelatin. Blends of gelatin, alginate and hyaluronic acid are promising candidates for the generation of non-toxic, biocompatible hydrogel scaffolds for tissue engineering. Variation of individual compound ratios in the blends can be used for a precise control of mechanical properties and may allow wide-ranging uses in various tissue engineering applications with different mechanical requirements.
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Alginatos/síntesis química , Gelatina/síntesis química , Ácido Hialurónico/síntesis química , Hidrogeles , Metacrilatos/síntesis química , Ingeniería de Tejidos/métodos , Andamios del Tejido , Alginatos/efectos de la radiación , Animales , Animales Recién Nacidos , Adhesión Celular , Supervivencia Celular , Células Cultivadas , Gelatina/efectos de la radiación , Ácido Hialurónico/análogos & derivados , Ácido Hialurónico/efectos de la radiación , Espectroscopía de Resonancia Magnética , Metacrilatos/efectos de la radiación , Estructura Molecular , Miocitos Cardíacos/fisiología , Ratas , Ratas Sprague-Dawley , Reología , Factores de Tiempo , Rayos UltravioletaRESUMEN
The electrochemically triggered dissolution of noncontinuous polyelectrolyte assemblies presenting distinct nanomorphologies and its tuning by chemical cross-linking were monitored locally, in situ, by electrochemical atomic force microscopy. Poly-l-lysine and hyaluronic acid deposited layer-by-layer on indium tin oxide electrodes at specific experimental conditions formed well-defined nanostructures whose morphologies could be easily and precisely followed along the dissolution process. In addition to shrinkage of polyelectrolyte nanodroplets, ecAFM images revealed the faster dissolution of coalesced structures compared to droplet-like complexes, and the readsorption of dissolved polyelectrolytes onto slower dissolving neighboring structures. Covalently cross-linked PLL/HA assemblies dissolved only partially, and exhibited slower dissolution rates compared to native multilayers, with a clear dependence on the cross-link density. Tuning the electrochemical dissolution of polyelectrolyte multilayers through chemical cross-linking opens new prospects for future biomedical applications, such as the development of advanced drug or gene delivery platforms allowing for tightly controlled releases of different compounds at specific rates.