Solvent-free synthesis of biostable segmented polyurethane shape memory polymers for biomedical applications
文献情報
Maryam Ramezani, Mary Beth Browning Monroe
Biostable shape memory polymers that remain stable in physiological conditions are beneficial for user-defined shape recovery in response to a specific stimulus. For potential commercialization and biocompatibility considerations, biomaterial synthesis must be simple and scalable. Hence, a library of biostable and cytocompatible shape memory polymers with tunable thermomechanical properties based on hard segment content was synthesized using a solvent-free method. Polymer surface chemistry, thermomechanical and shape memory properties, and biostability were assessed. We also investigated the effects of processing methods on thermomechanical and shape memory properties. All polymers showed high glass transition temperatures (>50 °C), which indicates that their temporary shape could be preserved after implantation. Polymers also demonstrate high shape fixity (73–80%) and shape recovery (93–95%). Minimal mass loss (<5%) was observed in accelerated oxidative (20% H2O2) and hydrolytic (0.1 M NaOH) media. Additionally, minimal shape recovery (∼0%) occurred in programmed samples with higher hard segment content that were stored in degradation media. After 40 days of storage in media, programmed samples recovered their primary shapes upon heating to temperatures above their transition temperature. Annealing to above the polymer melting point and solvent casting of polymers improved shape memory and thermal properties. To enable their potential use as biomaterial scaffolds, fiber formation of synthesized polyurethanes was compared with those of samples synthesized using a previously reported solvent-based method. The new method provided polymers that can form fibrous scaffolds with improved mechanical and shape memory properties, which is attributed to the higher molecular weight and crystalline content of polymers synthesized using the new, solvent-free approach. These biostable segmented polyurethanes could be coupled with a range of components that respond to specific stimuli, such as enzymes, magnetic field, pH, or light, to enable a specific shape change response, which could be coupled with drug and/or bioactive material delivery in future work.
関連文献
Controlled biomimetic silica formation using star-shaped poly(l-lysine)
Qinrong Wang, Jun Yu, Yunsong Yan, Shaoqiang Xu, Fangfang Wang, Qingnan Li, Jinzhi Wang, Xin Zhang, Daojun Liu
DOI: 10.1039/C2PY20070H
Synthesis of 3,3,3-trifluoropropene telomers and their modification into fluorosurfactants
Frédéric Boschet, Georgi Kostov, Bruno Ameduri, Andrew Jackson, Bernard Boutevin
DOI: 10.1039/C1PY00394A
Investigations on the spermine provoked liquid crystalline phase behavior of high molecular weight DNA in the presence of alkali and alkaline earth metal ions
Neethu Sundaresan, Thresia Thomas, T. J. Thomas, C. K. S. Pillai
DOI: 10.1039/C1PY00302J
Visualization of poly(methyl methacrylate) (PMMA) grafts on cellulose via high-resolution FT-IR microscopy imaging
Susanne Hansson, Thomas Tischer, Anja S. Goldmann, Anna Carlmark, Christopher Barner-Kowollik, Eva Malmström
DOI: 10.1039/C1PY00338K
Upgrading of bio-oil and subsequent co-processing under FCC conditions for fuel production
Udo Armbruster, Hanan Atia, Ursula Bentrup, Binh Minh Quoc Phan, Reinhard Eckelt, Luong Huu Nguyen, Duc Anh Nguyen, Andreas Martin
DOI: 10.1039/C5RE00068H
Terminal functional glycopolymersvia a combination of catalytic chain transfer polymerisation (CCTP) followed by three consecutive click reactions
Qiang Zhang, Stacy Slavin, Mathew W. Jones, Alice J. Haddleton, David M. Haddleton
DOI: 10.1039/C2PY20013A
Aqueous RAFT/MADIXpolymerisation of N-vinyl pyrrolidone at ambient temperature
Aymeric Guinaudeau, Stéphane Mazières, D. James Wilson, Mathias Destarac
DOI: 10.1039/C1PY00373A
Novel optically active helical poly(N-propargylthiourea)s: synthesis, characterization and complexing ability toward Fe(iii) ions
Ci Song, Lei Li, Fangjie Wang, Jianping Deng, Wantai Yang
DOI: 10.1039/C1PY00457C
Cationic polyesters bearing pendent amino groups prepared by thiol–ene chemistry
Vincent Darcos, Sarah Antoniacomi, Cédric Paniagua, Jean Coudane
DOI: 10.1039/C1PY00414J
こちらもおすすめ
N-乙酰基-L-精氨酸はどのように合成されますか?
N-乙酰基-L-精氨酸は、L-精氨酸をエタノールと酸化アクリル酸で反応させて得られます。この合成過程では、酸化アクリル酸がL-精氨酸のN-アミノグループに結合す...
カウウェルパリミタートを含む廃棄物はどのように処理すべきですか?
カウウェルパリミタートの廃棄物は、化学廃棄物として適切に収集し、専門的な廃棄処理業者に委託します。処理には、有害物質の除去と環境への影響最小化が重要です。温度は...
タテライル1,4,8,11-テトラエチルアセートの代替品はありますか?
タテライル1,4,8,11-テトラエチルアセートの代替品として、他のエチルエステル化合物や、有機窒素化合物が考えられます。ただし、代替品の選択は目的や使用条件に...
異丁卡因を取り扱う際の実験室安全事項は何ですか?
異丁卡因は毒性があり、皮膚や目を刺激する可能性があります。作業中は保護目鏡、防護手袋、防護マスクを使用し、ドラフトチャンバーで扱うべきです。漏えいした場合、その...
4-氯-2-丙基吡啶を取り扱う際の実験室安全事項は何ですか?
4-氯-2-丙基吡啶は有毒で、吸入や皮膚接触を避けることが重要です。PPEとしてゴーグル、マスク、長袖のガウン、手袋を使用し、ドラフトチャンバーを用いて操作しま...
9,10-脱水阿霉素について適用される法規ガイドラインは何ですか?
CAS番号80996-23-2の9,10-脱水阿霉素は、GHS分類においては第3類毒性物質に分類され、REACH規則においてはカテゴリー1の急性毒性物質とされて...
4-(3-溴苯基)噻唑-2-甲酸の物理化学的性質は何ですか?
4-(3-溴苯基)噻唑-2-甲酸の分子量は265.01です。この化合物は水に微溶です。反応性は中程度で、酸性やアルカリ性の条件下で分解する可能性があります。
3-(4-塩素フェニル)-3-オキセタニアミン塩酸塩はどの業界で使用されていますか?
3-(4-塩素フェニル)-3-オキセタニアミン塩酸塩は、医薬業界、ポリマー業界、センサー業界、半導体業界などで使用されています。この化合物は薬物開発の一部として...
氮卓斯汀杂质Eを取り扱う際の実験室安全事項は何ですか?
氮卓斯汀杂质E(CAS番号: 20526-97-0)を扱う際は、ゴーグルとシールド付きの手袋を使用し、漏洩がある場合はドラフトチャンバーを使用して処理することを...
デシシボチル-n-ブチルボルテゾミブはどのように保存すればよいですか?
デシシボチル-n-ブチルボルテゾミブは室温で保管し、直日光から遠ざけて密栓容器に保管することが推奨されます。
掲載誌
Journal of Materials Chemistry B

Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. The journals have a strong history of publishing quality reports of interest to interdisciplinary communities and providing an efficient and rigorous service through peer review and publication. The journals are led by an international team of Editors-in-Chief and Associate Editors who are all active researchers in their fields. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C. More than one Journal of Materials Chemistry journal may be suitable for certain fields and researchers are encouraged to submit their paper to the journal that they feel best fits for their particular article. Example topic areas within the scope of Journal of Materials Chemistry B are listed below. This list is neither exhaustive nor exclusive. Antifouling coatings Biocompatible materials Bioelectronics Bioimaging Biomimetics Biomineralisation Bionics Biosensors Diagnostics Drug delivery Gene delivery Immunobiology Nanomedicine Regenerative medicine & Tissue engineering Scaffolds Soft robotics Stem cells Therapeutic devices image block All articles published in Journal of Materials Chemistry B from 2019 onwards will be indexed in MEDLINE®. Articles that primarily focus on providing insight into the underlying science and performance of biomaterials within a biological environment are more suited to our companion journal, Biomaterials Science.










![2-Methyl-2-propanyl [1-(3-nitro-2-pyridinyl)-4-piperidinyl]carbamate structure 2-Methyl-2-propanyl [1-(3-nitro-2-pyridinyl)-4-piperidinyl]carbamate structure](https://static.chemtradehub.com/structs/833/833452-36-1-7af5.webp)
![4-[2-(3,4-Dihydro-2H-chromen-6-yl)-1,3-oxazol-5-yl]-1-(3-{[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl}benzyl)pyridinium bromide structure 4-[2-(3,4-Dihydro-2H-chromen-6-yl)-1,3-oxazol-5-yl]-1-(3-{[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl}benzyl)pyridinium bromide structure](https://static.chemtradehub.com/structs/155/155863-03-9-8183.webp)


![(3aR,7R,7aR)-2,2-Diethyl-3a,6,7,7a-tetrahydro-7-[(methylsulfonyl)oxy]-1,3-benzodioxole-5-carboxylic Acid Ethyl Ester structure (3aR,7R,7aR)-2,2-Diethyl-3a,6,7,7a-tetrahydro-7-[(methylsulfonyl)oxy]-1,3-benzodioxole-5-carboxylic Acid Ethyl Ester structure](https://static.chemtradehub.com/structs/204/204254-90-0-7172.webp)