Recent advances in composite hydrogels: synthesis, classification, and application in the treatment of bone defects
文献情報
Pengfei Zhang, Jin Qi, Ran Zhang, Yifan Zhao, Jingyu Yan, Yajuan Gong, Xiaoming Liu, Binbin Zhang, Xiao Wu, Xiuping Wu, Cheng Zhang, Bing Zhao, Bing Li
Bone defects are often difficult to treat due to their complexity and specificity, and therefore pose a serious threat to human life and health. Currently, the clinical treatment of bone defects is mainly surgical. However, this treatment is often more harmful to patients and there is a potential risk of rejection and infection. Hydrogels have a unique three-dimensional structure that can accommodate a variety of materials, including particles, polymers and small molecules, making them ideal for treating bone defects. Therefore, emerging composite hydrogels are considered one of the most promising candidates for the treatment of bone defects. This review describes the use of different types of composite hydrogel in the treatment of bone defects. We present the basic concepts of hydrogels, different preparation techniques (including chemical and physical crosslinking), and the clinical requirements for hydrogels used to treat bone defects. In addition, a review of numerous promising designs of different types of hydrogel doped with different materials (e.g., nanoparticles, polymers, carbon materials, drugs, and active factors) is also highlighted. Finally, the current challenges and prospects of composite hydrogels for the treatment of bone defects are presented. This review will stimulate research efforts in this field and promote the application of new methods and innovative ideas in the clinical field of composite hydrogels.
おすすめジャーナル

Current Opinion in Solid State & Materials Science

Acta Materialia

Current Opinion in Colloid & Interface Science

Nature Medicine

Russian Journal of Applied Chemistry

Russian Journal of Coordination Chemistry

Russian Chemical Bulletin

Russian Journal of Organic Chemistry

Journal of Peptide Science

Russian Journal of Bioorganic Chemistry
関連文献
Synthesis of functionalized cyclic carbonate monomers using a versatile pentafluorophenyl carbonate intermediate
Daniel P. Sanders, Daniel J. Coady, Manabu Yasumoto, Masaki Fujiwara, Haritz Sardon, James L. Hedrick
DOI: 10.1039/C3PY01128C
Precise evaluation of the block copolymer nanoparticle growth in polymerization-induced self-assembly under dispersion conditions
Yang Su, Xin Xiao, Shentong Li, Meihan Dan, Xiaohui Wang, Wangqing Zhang
DOI: 10.1039/C3PY00995E
Soluble and stable alternating main-chain merocyanine copolymers through quantitative spiropyran–merocyanine conversion
Hartmut Komber, Stefan Müllers, Alexander Held, Michael Walter
DOI: 10.1039/C3PY00853C
Sunlight induced atom transfer radical polymerization by using dimanganese decacarbonyl
Mustafa Ciftci
DOI: 10.1039/C3PY01009K
Nitroxide mediated polymerization of methacrylates at moderate temperature
Christophe Detrembleur, Christine Jérôme, Julien De Winter, Pascal Gerbaux, Jean-Louis Clément, Yohann Guillaneuf, Didier Gigmes
DOI: 10.1039/C3PY01133J
pH-sensitive pullulan-based nanoparticles for intracellular drug delivery
Yinsong Wang, Yang Liu, Yuanyuan Liu, Yan Wang, Jing Wu, Rongshan Li, Jinrong Yang
DOI: 10.1039/C3PY00817G
Polyoxalates from biorenewable diols via Oxalate Metathesis Polymerization
John J. Garcia, Stephen A. Miller
DOI: 10.1039/C3PY01185B
Microporous organic polymers with acetal linkages: synthesis, characterization, and gas sorption properties
Li-Min Zhang, Tao Wang, Bao-Hang Han
DOI: 10.1039/C3PY00854A
Superheated high-temperature size-exclusion chromatography with chloroform as the mobile phase for π-conjugated polymers
Xianwen Lou, Joost L. J. van Dongen, Yasmine Braeken, Jeroen Brebels, Gijs W. P. van Pruissen, Weiwei Li, Martijn M. Wienk, René A. J. Janssen
DOI: 10.1039/C3PY00933E
Self-activation and activation of Cu(0) wire for SET-LRP mediated by fluorinated alcohols
Shampa R. Samanta, Hao-Jan Sun, David M. Haddleton, Virgil Percec
DOI: 10.1039/C3PY01007D
こちらもおすすめ
「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか?
CAS番号163217-74-1の「邻羟基阿托伐他汀内酯标准品」は、GHS分類では危険物に分類されず、主にREACH規則とFDA/EPAの管理対象となります。R...
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか?
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩は、医薬品や合成化学の研究に広く用いられます。また、特定の薬物の前...
トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか?
トランス-4-メチルピロリジン-3-オール塩酸塩は、4-メチルピロリジンの塩酸塩化によって合成されます。一般的な合成方法では、4-メチルピロリジンを塩酸に加えて...
硫雜環丁烷-1,1-二氧化物は安全ですか?
硫雜環丁烷-1,1-二氧化物は安全ではありません。毒性は報告されていませんが、高温下で分解し、可燃性があるため、高圧ガスは注意が必要です。密閉した容器で保管し、...
9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか?
9-ヒドロキシエリプチシネ塩酸塩は、エリプチシネから塩酸を添加することで合成されます。選択性は高いですが、収率は約70%です。
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか?
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮のCAS番号は5621-86-3です。この化合物は白色の結晶性粉末で、分子量は415.03で...
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか?
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪は、直射日光を避けて暗所に、室温(15-25℃)で保管し、密閉容器に入れることで安定性を保つことができます。
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか?
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンは、医薬品の合成、有機合成化学、および新材料の研究で使用され...
掲載誌
Biomaterials Science

Biomaterials Science is an international high impact journal exploring the science of biomaterials and their translation towards clinical use. Its scope encompasses new concepts in biomaterials design, studies into the interaction of biomaterials with the body, and the use of materials to answer fundamental biological questions. Papers do not necessarily need to report a new biomaterial but should provide novel insight into the biological applications of the biomaterial. Articles that primarily focus on demonstrating novel materials chemistry and bring a molecular picture to bear on a given material’s suitability as a biomaterial are more suited to our companion journal, Journal of Materials Chemistry B. Biomaterials Science publishes primary research and review-type articles in the following areas: molecular design of biomaterials, including translation of emerging chemistries to biomaterials science of cells and materials at the nanoscale and microscale materials as model systems for stem cell and human biology materials for tissue engineering and regenerative medicine (Nano)materials and (nano)systems for therapeutic delivery interactions at the biointerface biologically inspired and biomimetic materials, including bio-inspired self-assembly systems and cell-inspired synthetic tools next-generation biomaterials tools and methods


![(2E)-3-(3-Chlorophenyl)-N-{2-[4-(methylsulfonyl)-1-piperazinyl]-2-oxoethyl}acrylamide structure (2E)-3-(3-Chlorophenyl)-N-{2-[4-(methylsulfonyl)-1-piperazinyl]-2-oxoethyl}acrylamide structure](https://static.chemtradehub.com/structs/250/2505001-54-5-c1e9.webp)

