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1.
Int J Biol Macromol ; 190: 607-617, 2021 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-34508721

RESUMO

Bone morphogenic protein-2/4 (BMP-2/4) is an osteoinductive protein that accelerates osteogenesis when administered to bony defects. Sericin is produced by silkworms, and has a biological activity that differs depending on the degumming method used. Our results indicated that the high molecular weight fraction of silk sericin (MW > 30 kDa) obtained via sonication had a more abundant ß-sheet structure than the low molecular weight fraction. Administration of the ß-sheet structure silk sericin increased BMP-2/4 expression in a dose-dependent manner in RAW264.7 cells and human monocytes. This sericin increased the expression levels of toll-like receptor (TLR)-2, TLR-3, and TLR-4 in RAW264.7 cells. Application of a TLR-2 antibody or TLR pathway blocker decreased BMP-2/4 expression following sericin administration. In the animal model, the bone volume and BMP-2/4 expression were higher in rats treated with a sericin-incorporated gelatin sponge than in rats treated with a gelatin sponge alone or a sponge-incorporated with denatured sericin. In conclusion, sericin with a more abundant ß-sheet structure increased BMP-2/4 expression and bone formation better than sericin with a less abundant ß-sheet structure.


Assuntos
Proteína Morfogenética Óssea 2/metabolismo , Proteína Morfogenética Óssea 4/metabolismo , Sericinas/farmacologia , Transdução de Sinais , Seda/química , Receptores Toll-Like/metabolismo , Animais , Bombyx , Regeneração Óssea/efeitos dos fármacos , Gelatina/química , Camundongos , Peso Molecular , Osteoblastos/efeitos dos fármacos , Osteoblastos/metabolismo , Conformação Proteica , Estrutura Secundária de Proteína , Células RAW 264.7 , Ratos Sprague-Dawley , Sericinas/química , Sericinas/isolamento & purificação , Transdução de Sinais/efeitos dos fármacos , Espectroscopia de Infravermelho com Transformada de Fourier , Temperatura , Microtomografia por Raio-X
2.
J Nanobiotechnology ; 19(1): 30, 2021 Jan 22.
Artigo em Inglês | MEDLINE | ID: mdl-33482828

RESUMO

BACKGROUND: The advances in products based on nanotechnology have directed extensive research on low-cost, biologically compatible, and easily degradable materials. MAIN BODY: Sericin (SER) is a protein mainly composed of glycine, serine, aspartic acid, and threonine amino acids removed from the silkworm cocoon (particularly Bombyx mori and other species). SER is a biocompatible material with economic viability, which can be easily functionalized due to its potential crosslink reactions. Also, SER has inherent biological properties, which makes possible its use as a component of pharmaceutical formulations with several biomedical applications, such as anti-tumor, antimicrobials, antioxidants and as scaffolds for tissue repair as well as participating in molecular mechanisms attributed to the regulation of transcription factors, reduction of inflammatory signaling molecules, stimulation of apoptosis, migration, and proliferation of mesenchymal cells. CONCLUSION: In this review, the recent innovations on SER-based nano-medicines (nanoparticles, micelles, films, hydrogels, and their hybrid systems) and their contributions for non-conventional therapies are discussed considering different molecular mechanisms for promoting their therapeutic applications.


Assuntos
Materiais Biocompatíveis/química , Materiais Biocompatíveis/uso terapêutico , Nanoestruturas/química , Sericinas/química , Sericinas/uso terapêutico , Animais , Materiais Biocompatíveis/isolamento & purificação , Materiais Biocompatíveis/farmacologia , Bombyx/química , Sistemas de Liberação de Medicamentos/métodos , Humanos , Nanomedicina/métodos , Nanotecnologia/métodos , Sericinas/isolamento & purificação , Sericinas/farmacologia , Alicerces Teciduais/química
3.
Biomed Res Int ; 2020: 9689386, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33204730

RESUMO

Sericin is a natural protein component of silks of silkworm and has potential utility in multiple areas such as pharmacological, cosmetics, and biotechnological industries. However, the understanding of its toxicological safety is still limited. This study evaluated the safety of water-extract sericin from silkworm (Bombyx mori) cocoons using different model approaches, including three genotoxicity studies (the bacterial reverse mutation test, the mammalian erythrocyte micronucleus test, and the mouse spermatogonia chromosomal aberration test) and a 90-day subchronic toxicity study in Sprague-Dawley (SD) rats. The results of this study showed that water-extract sericin was nonmutagenic and nongenotoxic both in vitro and in vivo. Sericin did not induce significant changes in the body and organ weight, food intake, blood hematology and serum biochemistry, urine index, and histopathology in rats. The NOAEL of sericin was determined to be 1 g/kg/day for male and female rats. These results indicated that water-extract sericin was of low toxicity in the experimental conditions of the current study and had the potential for application in food-related products.


Assuntos
Bombyx/química , Sericinas/toxicidade , Administração Oral , Animais , Análise Química do Sangue , Feminino , Rim/efeitos dos fármacos , Rim/patologia , Fígado/efeitos dos fármacos , Fígado/patologia , Masculino , Camundongos , Testes de Mutagenicidade , Tamanho do Órgão/efeitos dos fármacos , Ratos Sprague-Dawley , Salmonella typhimurium/efeitos dos fármacos , Salmonella typhimurium/genética , Sericinas/administração & dosagem , Sericinas/isolamento & purificação , Espermatogônias/efeitos dos fármacos , Espermatogônias/fisiologia , Testes de Toxicidade Subcrônica , Urinálise , Água/química
4.
Mater Sci Eng C Mater Biol Appl ; 108: 110400, 2020 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-31923995

RESUMO

Synthesis of hydroxyapatite (HAp) and sericin (SS) nanocomposites was carried out by a simple precipitation method performed in batch in a stirred tank reactor (ST). The reaction was achieved by mixing a solution of calcium chloride dihydrate, in which SS was dissolved, with a solution of disodium hydrogen phosphate at 37 °C. Three experimental conditions were studied by varying the concentration of SS: HAp, HAp/SS1 (0.01 g/L of SS) and HAp/SS2 (1 g/L of SS). The chemical and physical properties of the resulting HAp/SS nanocomposites were studied using several techniques (Atomic Absorption Spectrometry, Ultraviolet-Visible Spectrophotometry, Fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), Selected area diffraction (SAED) and Thermogravimetric analysis (TGA)). pH profile was also monitored over time for each experimental condition. The results revealed that nano single-phased HAp was formed with both rod and plate-like shape. Additionally, the particles have low crystallinity, characteristic similar to biological HAp. Regarding the influence of SS, one observed that with increasing SS concentration there is an increase in the mean particle size and the number of plate-like particles, as well as an increase in the aggregation degree and a decrease of the crystallinity. Further, the composites obtained have an inorganic/organic composition comparable to bone. Finally, in vitro cytotoxicity showed that the synthetized nanoparticles are non-toxic and cell viability is higher for HAp and HAp/SS samples when compared to a commercially available HAp. The produced materials can thus be considered suitable candidates for bone related applications.


Assuntos
Durapatita/química , Nanocompostos/química , Sericinas/farmacologia , Animais , Biomineralização , Bombyx/química , Precipitação Química , Desenho de Equipamento , Fibroblastos/efeitos dos fármacos , Humanos , Concentração de Íons de Hidrogênio , Nanocompostos/toxicidade , Sericinas/química , Sericinas/isolamento & purificação , Espectrofotometria Ultravioleta , Espectroscopia de Infravermelho com Transformada de Fourier , Temperatura , Termogravimetria , Difração de Raios X
5.
Nanotechnology ; 29(33): 335301, 2018 Aug 17.
Artigo em Inglês | MEDLINE | ID: mdl-29808832

RESUMO

Nanofabrication approaches to pattern proteins at the nanoscale are useful in applications ranging from organic bioelectronics to cellular engineering. Specifically, functional materials based on natural polymers offer sustainable and environment-friendly substitutes to synthetic polymers. Silk proteins (fibroin and sericin) have emerged as an important class of biomaterials for next generation applications owing to excellent optical and mechanical properties, inherent biocompatibility, and biodegradability. However, the ability to precisely control their spatial positioning at the nanoscale via high throughput tools continues to remain a challenge. In this study electron beam lithography (EBL) is used to provide nanoscale patterning using methacrylate conjugated silk proteins that are photoreactive 'photoresists' materials. Very low energy electron beam radiation can be used to pattern silk proteins at the nanoscale and over large areas, whereby such nanostructure fabrication can be performed without specialized EBL tools. Significantly, using conducting polymers in conjunction with these silk proteins, the formation of protein nanowires down to 100 nm is shown. These wires can be easily degraded using enzymatic degradation. Thus, proteins can be precisely and scalably patterned and doped with conducting polymers and enzymes to form degradable, organic bioelectronic devices.


Assuntos
Elétrons , Fibroínas/química , Nanofios/química , Poliestirenos/química , Impressão/métodos , Sericinas/química , Tiofenos/química , Animais , Biodegradação Ambiental , Bombyx/química , Condutividade Elétrica , Fibroínas/isolamento & purificação , Metacrilatos/química , Microscopia Eletrônica de Varredura/métodos , Nanofios/ultraestrutura , Impressão/instrumentação , Sericinas/isolamento & purificação , Silício/química
6.
Int J Biol Macromol ; 106: 39-47, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-28774806

RESUMO

Electro-spun regenerated silk webs have been extensively studied for biomedical applications because of the simplicity of their fabrication methods However, the productivity of the electro-spinning process is low for web fabrication and the mechanical properties of the electro-spun silk web are not satisfactory, which restricts its commercialization. In this study, a new silk non-woven fabric was successfully fabricated by wetting and hot press treatments using the excellent binding characteristic of sericin. The effects of the press temperature and residual sericin content on the preparation, structure, and properties of the silk non-woven fabric were examined. A press temperature of 200°C was optimum for obtaining non-woven fabrics with best mechanical properties, without yellowing. The silk non-woven fabric could not be fabricated without sericin, and a minimum of 8% sericin was required to fabricate it. As the sericin content was increased, the strength and Young's modulus of the silk non-woven fabric increased, while the tensile elongation remained constant. Regardless of the press temperature and sericin content, all the silk non-woven fabrics showed good cell viability, comparable to that of the tissue culture plate (TCP) used as a control until 4days, which however decreased compared to that of TCP after 7days.


Assuntos
Sericinas/química , Têxteis/análise , Alicerces Teciduais , Animais , Bombyx , Sobrevivência Celular/efeitos dos fármacos , Módulo de Elasticidade , Temperatura Alta , Teste de Materiais , Camundongos , Células NIH 3T3 , Pressão , Sericinas/isolamento & purificação , Sericinas/farmacologia , Engenharia Tecidual
7.
Drug Res (Stuttg) ; 68(6): 317-327, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29132177

RESUMO

Silks are naturally occurring polymers that have been used clinically as sutures for hundreds of years. It's so for obtained from insects or worms, silk consists of a filament core protein, termed fibroin, and a glue-like coating made up of sericin proteins. An important component of silk has an extended history of being discarded as a waste in the course of silk processing. The cost of sericin for tissue engineering is underestimated and its capability in using as regenerative remedy has simply began to be explored. Its variable amino acid composition and various functional groups confer upon it attractive bioactive proteins, which are particularly interesting for biomedical programs. Because of its antioxidant properties, moisturizing ability, and mitogenic effect on mammalian cells, sericin is beneficial in cell regeneration and tissue engineering. Research shows that keratinocytes and fibroblasts have brought about the improvement of sericin-primarily based biomaterials for skin tissue repair, in particular as wound dressings. Moreover, sericin may be used for bone tissue engineering due to its ability to set off nucleation of bone-like hydroxyapatite. Stable silk sericin biomaterials, as films, sponges, and hydrogels, are obtained by means of cross-linking, ethanol precipitation, or mixing with different polymers. Now a day, sericin may also be used for delivery of drugs due to its chemical reactivity and pH-responsiveness which facilitate the fabrication of nano and microparticles, hydrogels, and conjugated molecules, enhancing the bioactivity of drugs. In this review, we outlined the current headways from extraction of sericin till its physical properties and biomedical applications.


Assuntos
Materiais Biocompatíveis/uso terapêutico , Sericinas/uso terapêutico , Engenharia Tecidual/métodos , Animais , Materiais Biocompatíveis/química , Materiais Biocompatíveis/farmacologia , Humanos , Sericinas/química , Sericinas/isolamento & purificação , Sericinas/farmacologia
8.
Biomacromolecules ; 18(6): 1937-1946, 2017 Jun 12.
Artigo em Inglês | MEDLINE | ID: mdl-28448131

RESUMO

Native silk fibers are known to demonstrate excellent mechanical properties such as high strength and ductility. However, regenerated silk material has not yet been used as a tough structural material in our everyday life. To recreate the mechanical properties with regenerated silk material, the network structure and hydration state of silk materials are studied and optimized in this study. This is the first to demonstrate the effect of chemical and physical cross-links in hydrated and dehydrated silk materials, namely, silk hydrogels and resins. Mild hydration conditions (relative humidity 20-60%) realizes tough and strong silk materials with chemical and physical cross-links. In the case of relatively high concentrations of silk molecules, contributions to the high strength and toughness of silk-based materials are considered to come not only from ß-sheet cross-links and chemical dityrosine links but also from entanglements and assembly via the hydrophobic interactions of silk molecules. In addition, dehydration treatment does not disturb the biodegradability of the silk resins in natural environments. Based on the overall results, the silk resins with controlled network structures and hydration state have successfully achieved the highest toughness possible for a bulk silk material while maintaining favorable biodegradability.


Assuntos
Hidrogéis/química , Sericinas/química , Seda/química , Animais , Bombyx/fisiologia , Reagentes de Ligações Cruzadas/química , Interações Hidrofóbicas e Hidrofílicas , Teste de Materiais , Sericinas/isolamento & purificação , Resistência à Tração , Água/química
9.
Acta Biomater ; 41: 210-23, 2016 09 01.
Artigo em Inglês | MEDLINE | ID: mdl-27262742

RESUMO

UNLABELLED: Acute myocardial infarction (MI) leads to morbidity and mortality due to cardiac dysfunction. Here we identify sericin, a silk-derived protein, as an injectable therapeutic biomaterial for the minimally invasive MI repair. For the first time, sericin prepared in the form of an injectable hydrogel has been utilized for cardiac tissue engineering and its therapeutical outcomes evaluated in a mouse MI model. The injection of this sericin hydrogel into MI area reduces scar formation and infarct size, increases wall thickness and neovascularization, and inhibits the MI-induced inflammatory responses and apoptosis, thereby leading to a significant functional improvement. The potential therapeutical mechanisms have been further analyzed in vitro. Our results indicate that sericin downregulates pro-inflammatory cytokines (TNF-α and IL-18) and chemokine (CCL2) and reduces TNF-α expression by suppressing the TLR4-MAPK/NF-κB pathways. Moreover, sericin exhibits angiogenic activity by promoting migration and tubular formation of human umbilical vessel endothelial cells (HUVECs). Also, sericin stimulates VEGFa expression via activating ERK phosphorylation. Further, sericin protects endothelial cells and cardiomyocytes from apoptosis by inhibiting the activation of caspase 3. Together, these diverse biochemical activities of sericin protein lead to a significant recovery of cardiac function. This work represents the first study reporting sericin as an effective therapeutic biomaterial for ischemic myocardial repair in vivo. STATEMENT OF SIGNIFICANCE: Intramyocardial biomaterial injection is thought to be a potential therapeutic approach to improve cardiac performance after ischemic myocardial infarction. In this study, we report the successful fabrication and in vivo application of an injectable sericin hydrogel for ischemic heart disease. We for the first time show that the injection of in situ forming crosslinked sericin hydrogel promotes heart functional recovery accompanied with reduced inflammatory responses, attenuated apoptosis and increased microvessel density in the infarcted hearts. Further, we reveal that the improvement in those aspects is ascribed to sericin protein's functional bioactivities that are comprehensively uncovered in this study. Thus, we identify sericin, a natural protein, as a biomaterial suitable for myocardial repair and demonstrate that the in vivo application of this injectable sericin hydrogel can be an effective strategy for treating MI.


Assuntos
Hidrogel de Polietilenoglicol-Dimetacrilato/farmacologia , Injeções , Infarto do Miocárdio/fisiopatologia , Recuperação de Função Fisiológica/efeitos dos fármacos , Sericinas/farmacologia , Animais , Apoptose/efeitos dos fármacos , Movimento Celular/efeitos dos fármacos , Reagentes de Ligações Cruzadas/farmacologia , Citocinas/metabolismo , Citoproteção/efeitos dos fármacos , Fibrose , Células Endoteliais da Veia Umbilical Humana/citologia , Inflamação/patologia , Iridoides/farmacologia , Sistema de Sinalização das MAP Quinases/efeitos dos fármacos , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Infarto do Miocárdio/patologia , Miócitos Cardíacos/citologia , Miócitos Cardíacos/efeitos dos fármacos , Células NIH 3T3 , Neovascularização Fisiológica/efeitos dos fármacos , Ratos , Sericinas/isolamento & purificação , Transcrição Gênica/efeitos dos fármacos , Fator A de Crescimento do Endotélio Vascular/genética , Fator A de Crescimento do Endotélio Vascular/metabolismo
10.
Biosci Biotechnol Biochem ; 80(2): 241-9, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26399155

RESUMO

Sericin was extracted from three strains of Thai Bombyx mori silk cocoons (white shell Chul1/1, greenish shell Chul3/2, and yellow shell Chul4/2) by a high-pressure and high-temperature technique. The characteristics of sericin extracted from different fractions (15, 45, and 60 min extraction process) were compared. No differences in amino acid composition were observed among the three fractions. For all silk strains, sericin extracted from a 15-min process presented the highest molecular weight. The biological potential of the different sericin samples as a bioadditive for 3T3 fibroblast cells was assessed. When comparing sericin extracted from three silk strains, sericin fractions extracted from Chul4/2 improved cell proliferation, while sericin from Chul 1/1 activated Type I collagen production to the highest extent. This study allows the natural variability of sericin obtained from different sources and extraction conditions to be addressed and provides clues for the selection of sericin sources.


Assuntos
Aminoácidos/química , Bombyx/genética , Proteínas de Insetos/química , Sericinas/química , Animais , Bombyx/metabolismo , Proliferação de Células/efeitos dos fármacos , Cromatografia de Fase Reversa , Expressão Gênica , Proteínas de Insetos/biossíntese , Proteínas de Insetos/isolamento & purificação , Proteínas de Insetos/farmacologia , Extração Líquido-Líquido/métodos , Camundongos , Peso Molecular , Células NIH 3T3 , Sericinas/biossíntese , Sericinas/isolamento & purificação , Sericinas/farmacologia , Fatores de Tempo
11.
Zhong Yao Cai ; 38(5): 915-8, 2015 May.
Artigo em Chinês | MEDLINE | ID: mdl-26767282

RESUMO

OBJECTIVE: To optimize the appropriate extracting technology for sericin from Silkworm cocoon. METHODS: Using sericin extraction rates and sericin content as the indices. The single and orthogonal experiments were used to determine the best conditions. RESULTS: The optimal extraction technology for sericin from Silkworm cocoon was as follows: 1: 30 for the ratio of solid to liquid, 3 h reflux for 2 times of extraction and water temperature at 100 degrees C. The extraction rate of sericin from Silkworm cocoon was 27.1%. CONCLUSION: The optimal extraction technology is stable, feasible, and can provide reference for further pharmacological study on cocoon sericin.


Assuntos
Bombyx , Sericinas/isolamento & purificação , Animais , Temperatura , Água
12.
Int J Biol Macromol ; 70: 70-7, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-24971560

RESUMO

Silk proteins of silkworms are chiefly composed of core fibroin protein and glycoprotein sericin that glues fibroin. Unique mechanical properties, cyto-compatibility and controllable biodegradability facilitate the use of fibroin in biomedical applications. Sericin serves as additive in cosmetic and food industries, as mitotic factor in cell culture media, anti-cancerous drug, anticoagulant and as biocompatible coating. For all these uses; aqueous solutions of silk proteins are preferred. Therefore, an accurate understanding of extraction procedure of silk proteins from their sources is critical. A number of protocols exist, amongst which it is required to settle a precise and easy one with desired yield and least down-stream processing. Here, we report extraction of proteins employing methods mentioned in literature using cocoons of mulberry and nonmulberry silks. This study reveals sodium carbonate salt-boiling system is the most efficient sericin extraction procedure for all silk variants. Lithium bromide is observed as the effective fibroin dissolution system for mulberry silk cocoons; whereas heterogeneous species-dependent result is obtained in case of nonmulberry species. We further show the effect of common post processing on nanoscale morphology of mulberry silk fibroin films. This knowledge eases the adoption and fabrication of silk biomaterials in devices and therapeutic delivery systems.


Assuntos
Proteínas de Insetos/química , Proteínas de Insetos/isolamento & purificação , Seda/química , Animais , Bombyx/metabolismo , Fibroínas/química , Fibroínas/isolamento & purificação , Sericinas/química , Sericinas/isolamento & purificação , Seda/ultraestrutura
13.
Tissue Eng Part C Methods ; 20(5): 431-9, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24066942

RESUMO

Silk fibroin has previously been described as a promising candidate for ligament tissue engineering (TE) approaches. For biocompatibility reasons, silkworm silk requires removal of sericin, which can elicit adverse immune responses in the human body. One disadvantage of the required degumming process is the alteration of the silk fiber structural properties, which can hinder textile engineering of high order hierarchical structures. Therefore, the aim of this study was to find a way to remove sericin from a compact and highly ordered raw silk fiber matrix. The wire rope design of the test model scaffold comprises several levels of geometric hierarchy. Commonly used degumming solutions fail in removing sericin in this wire rope design. Weight loss measurements, picric acid and carmine staining as well as scanning electron microscopy demonstrated that the removal of sericin from the model scaffold of a wire rope design can be achieved through a borate buffer-based system. Furthermore, the borate buffer degummed silks were shown to be nontoxic and did not alter cell proliferation behavior. The possibility to remove sericin after the textile engineering process has taken place eases the production of highly ordered scaffold structures and may expand the use of silk as scaffold material in further TE and regenerative medicine applications.


Assuntos
Bombyx/química , Sericinas/isolamento & purificação , Alicerces Teciduais/química , Animais , Soluções Tampão , Carmim/metabolismo , Morte Celular/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Fibroblastos/citologia , Fibroblastos/efeitos dos fármacos , Humanos , Peso Molecular , Picratos/metabolismo , Sericinas/farmacologia , Sericinas/ultraestrutura , Coloração e Rotulagem , Células Estromais/citologia , Células Estromais/efeitos dos fármacos , Resistência à Tração/efeitos dos fármacos
14.
Int J Biol Macromol ; 52: 59-65, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23026092

RESUMO

Although the technique for extracting the Bombyx mori sericin has been extensively known, the extraction of sericin from wild-silkworm cocoons is not yet standardized. The aim of this study was to find the optimal conditions for the extraction of sericin from Antheraea mylitta cocoons, with high yields and minimum degradation. We attempted to apply various protocols for the extraction of the A. mylitta sericin (AmS). Among these, we found that the extraction of AmS with a sodium carbonate solution exhibited the highest yield except the conventional soap-alkali extraction. To find the optimal conditions for the AmS extraction with the sodium carbonate, we changed the concentration of sodium carbonate and the treatment time. With an increase in the sodium carbonate concentration and the extraction time, the yield of AmS increased, but the molecular weight (MW) of AmS decreased. Considering the yield, molecular weight distribution (MWD) and amino acid composition of AmS, we suggest that the optimal conditions for the AmS extraction require treatment with 0.02 M sodium carbonate and boiling for 60 min.


Assuntos
Mariposas/química , Proteólise , Sericinas/isolamento & purificação , Animais , Sericinas/química
15.
Food Funct ; 3(2): 150-8, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22101964

RESUMO

The cocoon shell of the silkworm Bombyx mori consists of silk fibroin fiber (70%) surrounded by a sericin layer made up of sericin (25%) and non-sericin (5%) components. The non-sericin component which consists of carbohydrate, salt, wax, flavonoids and derivatives is often overlooked in applied research into sericin and its hydrolysate. Here, sericin and non-sericin compounds were obtained from the sericin layer of five types of cocoon shell by means of degumming in water followed by extraction and separation in ethanol. These ethanol extracts were found to mainly contain flavonoids and free amino acids possessing scavenging activities of the 2,2-diphenyl -1-picrylhydrazyl (DPPH) free radical and inhibiting activities of tyrosinase, which were much greater than the corresponding activities of the purified sericin proteins. The extracts also strongly inhibited α-glucosidase while the sericins had no such activity. In particular, the inhibitory activities of the ethanol extract of Daizo cocoons were much greater than those of the other cocoons. The IC(50) values of the Daizo cocoons for DPPH free radicals, tyrosinase, and α-glucosidase were 170, 27, and 110 µg mL(-1), respectively. The bioactivities of the non-sericin component were much higher than the activity of sericin alone. In addition, the in vivo test showed preliminarily that the administration of the non-sericin component had effectively resistant activity against streptozocin (STZ) oxidation and that of the purified sericin could also evidently decrease the induction ratio of diabetic mice induced by STZ. Therefore, ethanol extract protocols of the sericin layer of cocoon shells provide a novel stock which, together with sericin protein, has potential uses in functional food, biotechnological and medical applications.


Assuntos
Bombyx/química , Sericinas/química , Sericinas/isolamento & purificação , Seda/química , Animais , Compostos de Bifenilo/metabolismo , Diabetes Mellitus Experimental , Feminino , Fibroínas/metabolismo , Masculino , Camundongos , Monofenol Mono-Oxigenase/metabolismo , Picratos/metabolismo , alfa-Glucosidases/metabolismo
16.
Int J Biol Macromol ; 48(1): 32-7, 2011 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-20875446

RESUMO

In order to improve some inherent disadvantages in the mechanical properties of silk sericin (SS), we prepared ethanol-precipitated sericin (EpSS) by adding ethanol into hot-water extracted sericin (HS) solution. EpSS had higher viscosity compared to HS and it was due to the differences in their molecular weight distribution (MWD). The different MWD of EpSS was due to the different solubility of sericin molecules at various concentrations of ethanol, and the amino acid composition of EpSS showed that the more hydrophobic sericin is precipitated more readily in the presence of ethanol. The secondary structure of sericin is also changed from a random coil to ß-sheet structure when the amount of ethanol added is high enough. The DSC analysis also revealed that EpSSs has a more compact structure. Finally, when beads were prepared from EpSS, they had enhanced compressive strength compared to those from HS.


Assuntos
Precipitação Química , Etanol/química , Temperatura Alta , Sericinas/isolamento & purificação , Água/química , Aminoácidos/análise , Animais , Fenômenos Biomecânicos , Bombyx/química , Varredura Diferencial de Calorimetria , Dicroísmo Circular , Força Compressiva , Interações Hidrofóbicas e Hidrofílicas , Peso Molecular , Estrutura Secundária de Proteína , Sericinas/química , Solventes/química , Viscosidade
17.
Pharm Biol ; 48(8): 855-60, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20673171

RESUMO

Oils and sericin were extracted from pupae and silk cocoons, respectively, of the five Thai native silkworms (Bombyx mori, Linnaeus (Bombycidae)), namely, Keawsakol, Nangnoi, Somrong, Nangleung, and Noneruesee, which are variations of the same species. The oils were extracted by a hot process using Soxhlet apparatus and a cold process using petroleum ether, while sericin was extracted by basic hydrolysis and autoclaving. Sericin from the five Thai native silkworms showed free radical scavenging activity lower than the standard antioxidants (vitamin C, vitamin E, and BHT) by about 20-100-fold, but all oils gave higher activity than that of the standard linoleic acid by 11-22-fold. Oil extracted from Noneruesee by the cold process gave the highest DPPH scavenging activity, compared with other oil samples. All sericin samples showed tyrosinase inhibition activity with IC(50) values in the range of 1.2-18.76 mg/mL, but only oils from Noneruesee extracted by the hot process, and Nangleung, Somrong, and Noneruesee extracted by the cold process, showed this activity. Oil extracted by the hot process and sericin by basic hydrolysis from Noneruesee gave the highest tyrosinase inhibition activity, but lower than that of the standards vitamin C and kojic acid by 20-49 and 3-8 times, respectively. This study has suggested that sericin and oil from Noneruesee extracted by basic hydrolysis and the cold process, which gave the highest tyrosinase inhibition and free radical scavenging activity, respectively, can be applied in antiaging and whitening cosmetic products.


Assuntos
Bombyx , Sequestradores de Radicais Livres/isolamento & purificação , Monofenol Mono-Oxigenase/antagonistas & inibidores , Óleos/isolamento & purificação , Sericinas/isolamento & purificação , Animais , Inibidores Enzimáticos/química , Inibidores Enzimáticos/isolamento & purificação , Inibidores Enzimáticos/metabolismo , Sequestradores de Radicais Livres/química , Sequestradores de Radicais Livres/metabolismo , Monofenol Mono-Oxigenase/metabolismo , Óleos/química , Óleos/metabolismo , Sericinas/química , Sericinas/metabolismo , Tailândia
18.
Bioresour Technol ; 101(21): 8439-45, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20598526

RESUMO

Silk fibers from Bombyx mori silkworm was degummed with different concentration of citric acid, and the physical properties and fine structure were investigated to elucidate the effects of citric acid treatment. The silk sericin removal percentage was almost 100% after degumming with 30% citric acid which resulted in a total weight loss of 25.4% in the silk fibers. The surface morphology of silk fiber degummed with citric acid was very smooth and fine, showed perfect degumming like traditional soap-alkali method. The tensile strength of silk fiber was increased after degumming with citric acid (507MPa), where as the traditional soap-alkali method causes to decrease the strength about half of the control silk fiber (250MPa). The molecular conformation estimated by Fourier transform infrared spectroscopy and the crystalline structure evaluated from X-ray diffraction curve stayed unchanged regardless of the degumming with citric acid and soap. The dye uptake percentage of silk fiber degummed with citric acid decreased slightly, about 4.2%. On the other hand, the dye uptake percentage of silk degummed with soap was higher which indicates the disordering of the molecular orientation of the laterally ordered structure, accompanied with the partial hydrolysis of silk fibroin molecules by the alkali action of soap. The thermal properties were greatly enhanced by soap and citric acid degumming agents. Dynamic mechanical thermal analysis showed silk degummed with citric acid is more stable in higher temperature than that of soap. With heating at above 300 degrees C, the silk degummed with citric acid shows an increase in storage modulus and an onset of tan delta peaks at 325 degrees C and the melt flow of the sample was inhibited. The degumming of silk fibers with citric acid is safe and the results obtained are quite promising as a basis for possible future industrial application.


Assuntos
Ácido Cítrico/farmacologia , Corantes/química , Seda/química , Varredura Diferencial de Calorimetria , Módulo de Elasticidade/efeitos dos fármacos , Sericinas/isolamento & purificação , Seda/ultraestrutura , Espectroscopia de Infravermelho com Transformada de Fourier , Propriedades de Superfície/efeitos dos fármacos , Temperatura , Resistência à Tração/efeitos dos fármacos , Difração de Raios X
19.
Int J Mol Sci ; 11(5): 2200-11, 2010 May 20.
Artigo em Inglês | MEDLINE | ID: mdl-20559510

RESUMO

Silk sericin (SS) can accelerate cell proliferation and attachment; however, SS can be extracted by various methods, which result in SS exhibiting different physical and biological properties. We found that SS produced from various extraction methods has different molecular weights, zeta potential, particle size and amino acid content. The MTT assay indicated that SS from all extraction methods had no toxicity to mouse fibroblast cells at concentrations up to 40 mug/mL after 24 h incubation, but SS obtained from some extraction methods can be toxic at higher concentrations. Heat-degraded SS was the least toxic to cells and activated the highest collagen production, while urea-extracted SS showed the lowest cell viability and collagen production. SS from urea extraction was severely harmful to cells at concentrations higher than 100 mug/mL. SS from all extraction methods could still promote collagen production in a concentration-dependent manner, even at high concentrations that are toxic to cells.


Assuntos
Colágeno/biossíntese , Fibroblastos/metabolismo , Sericinas , Animais , Linhagem Celular , Sobrevivência Celular/efeitos dos fármacos , Relação Dose-Resposta a Droga , Fibroblastos/citologia , Camundongos , Sericinas/química , Sericinas/isolamento & purificação , Sericinas/farmacologia , Ureia/química
20.
Biomed Mater ; 5(3): 35008, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20460689

RESUMO

In the process of removing sericin (degumming) from a raw silk scaffold, the fibroin structural integrity is often challenged, leading to mechanical depreciation. This study aims to identify the factors and conditions contributing to fibroin degradation during alkaline degumming and to perform an optimization study of the parameters involved to achieve preservation of fibro in structure and properties. The methodology involves degumming knitted silk scaffolds for various durations (5-90 min) and temperatures (60-100 ◦C). Mechanical agitation and use of the refreshed solution during degumming are included to investigate how these factors contribute to degumming efficiency and fibroin preservation. Characterizations of silk fibroin morphology, mechanical properties and protein components are determined by scanning electron microscopy (SEM), single fiber tensile tests and gel electrophoresis (SDS­PAGE),respectively. Sericin removal is ascertained via SEM imaging and a protein fractionation method involving SDS­PAGE. The results show that fibroin fibrillation, leading to reduced mechanical integrity, is mainly caused by prolonged degumming duration. Through a series of optimization, knitted scaffolds are observed to be optimally degummed and experience negligible mechanical and structural degradation when subjected to alkaline degumming with mechanical agitation for 30 min at 100 ◦C.


Assuntos
Materiais Biocompatíveis/síntese química , Fibroínas/química , Fibroínas/ultraestrutura , Sericinas/química , Sericinas/isolamento & purificação , Alicerces Teciduais , Calefação/métodos , Teste de Materiais , Tamanho da Partícula , Conformação Proteica , Estresse Mecânico , Resistência à Tração
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