Preparation of berberine-naringin dual drug-loaded composite microspheres and evaluation of their antibacterial-osteogenic properties / 中国修复重建外科杂志

OBJECTIVE@#To develop a drug-loaded composite microsphere that can simultaneously release the berberine (BBR) and naringin (NG) to repair infectious bone defects.@*METHODS@#The NG was loaded on mesoporous microspheres (MBG) to obtain the drug-loaded microspheres (NG-MBG). Then the dual drug-loaded compound microspheres (NG-MBG@PDA-BBR) were obtained by wrapping NG-MBG with polydopamine (PDA) and modifying the coated PDA with BBR. The composite microspheres were characterized by scanning electron microscopy, X-ray diffraction, specific surface area and pore volume analyzer, and Fourier transform infrared spectroscopy; the drug loading rate and release of NG and BBR were measured; the colony number was counted and the bacterial inhibition rate was calculated after co-culture with Staphylococcus aureus and Escherichia coli for 12 hours to observe the antibacterial effect; the biocompatibility was evaluated by live/dead cell fluorescence staining and cell counting kit 8 assay after co-culture with rat's BMSCs for 24 and 72 hours, respectively, and the osteogenic property was evaluated by alkaline phosphatase (ALP) staining and alizarin red staining after 7 and 14 days, respectively.@*RESULTS@#NG-MBG@PDA-BBR and three control microspheres (MBG, MBG@PDA, and NG-MBG@PDA) were successfully constructed. Scanning electron microscopy showed that NG-MBG@PDA-BBR had a rough lamellar structure, while MBG had a smooth surface, and MBG@PDA and NG-MBG@PDA had a wrapped agglomeration structure. Specific surface area analysis showed that MBG had a mesoporous structure and had drug-loading potential. Low angle X-ray diffraction showed that NG was successfully loaded on MBG. The X-ray diffraction pattern contrast showed that all groups of microspheres were amorphous. Fourier transform infrared spectroscopy showed that NG and BBR peaks existed in NG-MBG@PDA-BBR. NG-MBG@PDA-BBR had good sustained drug release ability, and NG and BBR had early burst release and late sustained release. NG-MBG@PDA-BBR could inhibit the growth of Staphylococcus aureus and Escherichia coli, and the antibacterial ability was significantly higher than that of MBG, MBG@PDA, and NG-MBG@PDA ( P<0.05). But there was a significant difference in biocompatibility at 72 hours among microspheres ( P<0.05). ALP and alizarin red staining showed that the ALP positive area and the number of calcium nodules in NG-MBG@PDA-BBR were significantly higher than those of MBG and NG-MBG ( P<0.05), and there was no significant difference between NG-MBG@PDA and NG-MBG@PDA ( P>0.05).@*CONCLUSION@#NG-MBG@PDA-BBR have sustained release effects on NG and BBR, indicating that it has ideal dual performance of osteogenesis and antibacterial property.

Evaluation of wettability characteristics and adhesion of resin composite to photo-polymerized pulp-capping materials with and without bioactive glass / Avaliação das características de molhabilidade e adesão da resina composta aos materiais fotopolimerizáveis com e sem vidro bioativo

Objective: This study evaluated the wettability and adhesive properties of three different photopolymerized resin-based pulp-capping materials with or without bioactive glass (BAG). Material and Methods: Cylindrical specimens (5 per group) were prepared from photo-polymerized pulp-capping materials (TER-TheraCal LC, BIN-Biner LC, and CAL-CalciPlus LC containing BAG). After surface finishing, contact angle measurements were made (θ)using the sessile drop method and surface free energy was calculated. For shear test, cylindrical acrylic blocks (N = 30) (diameter: 6 mm; height: 1 m) in the center were filled with the pulp-capping materials (N = 10 per group) flattened using a metal spatula and photo-polymerized. The specimens were stored at 37 °C in 100% humidity for 24 h prior to the bonding procedures. An adhesive system (CLEARFIL SE BOND, Kuraray) was applied on the material surfaces and photo-polymerized for 20 s. Then, resin composite material (Filtek Z250, 3M ESPE) was bonded on the substrate materials using translucent plastic molds (internal diameter: 2 mm; height: 2 mm). The specimens were photopolymerized with an LED photo-polymerization unit for 20 s. After polymerization, the specimens were stored at 37 °C, at 100% humidity for 24 h. Shear force was applied at the pulp-capping material and the resin composite interface In a universal testing machine (1 mm/min).Data were analyzed using 1-way ANOVA and Tukey`s tests at the significance level of 0.05. Results: Contact angle values showed significant difference between the 3 materials with group CAL presenting the lowest (35.35 ± 12.89) and group BIN the highest values (74.77 ± 13.56) (p < 0.05). Significantly lower surface energy was observed with BIN (36.22) (p 0.05). Group BIN (9.12 ± 3.45) showed significantly lower (p < 0.05) mean bond strength than those of TER (11.56 ± 5.67) and CAL (12.66 ± 4.34) (p > 0.05). Most of the observed modes of failures in all groups were of mixed type of failures. Conclusion: The bioglass used in Calciplus LC did not adversely affect the wettability, surface energy and adhesive properties. (AU)

Objetivo: Este estudo avaliou as propriedades de molhabilidade e adesivas de três diferentes materiais capeadores pulpares fotopolimerizaveis à base de resina, com ou sem vidro bioativo (BAG). Material e Métodos: Amostras cilíndricas (5 por grupo) foram preparadas a partir de materiais capeadores pulpares fotopolimerizáveis (TER-TheraCal LC, BIN-Biner LC e CAL-CalciPlus LC contendo BAG). Após o acabamento da superfície, as medidas do ângulo de contato foram feitas (θ) usando o método de gota séssil e a energia livre da superfície foi calculada. Para o ensaio de cisalhamento, blocos de acrílico cilíndricos (N = 30) (diâmetro: 6 mm; altura: 1 m) foram preenchidos no centro com os materiais de capeamento pulpar (N = 10 por grupo) achatados usando uma espátula metálica e fotopolimerizados. Os espécimes foram armazenados a 37 ° C em 100% de umidade por 24 h antes dos procedimentos de colagem. Um sistema adesivo (CLEARFIL SE BOND, Kuraray) foi aplicado nas superfícies do material e fotopolimerizado por 20 segundos. Em seguida, o material de resina composta (Filtek Z250, 3M ESPE) foi colado nos materiais do substrato utilizando moldes de plástico translúcido (diâmetro interno: 2 mm; altura: 2 mm). Os espécimes foram fotopolimerizados com um dispositivo de fotopolimerização de LED por 20 s. Após a polimerização, os espécimes foram armazenados a 37 °C, a 100% de umidade por 24 h. A força de cisalhamento foi aplicada no material capeador e na interface da resina composta em uma máquina universal de ensaios (1 mm / min). Os dados foram analisados por meio do teste de ANOVA e teste de Tukey ao nível de significância de 0,05. Resultados: Os valores do ângulo de contato mostraram diferença significativa entre os 3 materiais com o grupo CAL apresentando os menores valores (35,35 ± 12,89) e o grupo BIN os maiores valores (74,77 ± 13,56) (p < 0,05). Uma energia de superfície significativamente menor foi observada com o BIN (36,22) (p 0,05). O grupo BIN (9,12 ± 3,45) apresentou resistência de união média significativamente menor (p 0,05). A maioria dos modos de falhas observados em todos os grupos eram de tipo misto de falhas. Conclusão: O biovidro utilizado no Calciplus LC não afetou negativamente a molhabilidade, energia superficial e propriedades adesivas. (AU)