Добавил:
Sekretar
kiopkiopkiop18@yandex.ru
t.me/Prokururor I Вовсе не секретарь, но почту проверяю
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз:
Предмет:
Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5463_Библиотеки_им_академика_М_И_Перельмана.pdf
X
- •About the Editor
- •Contents
- •Contributors
- •1.1.4 Components of niosome
- •1.1.5 Factors affecting niosomes
- •Preface
- •Abstract
- •1.1 Introduction
- •1.1.1 Why niosome?
- •1.1.2 Advantages of niosome
- •1.1.3 Structure of niosome
- •1.2 Applications of niosome
- •1.2.2 Niosomes for the delivery of therapeutics
- •1.2.3 Niosomes in biomedical applications
- •1.3 Conclusions and future prospects
- •Keywords
- •References
- •Abstract
- •2.1 Introduction
- •2.2 Conclusions
- •Acknowledgments
- •Keywords
- •References
- •Abstract
- •3.1 Introduction
- •3.2.1 Parameters involved in electrospinning process
- •3.2.2 Biomaterials for electrospinning
- •3.3 Electrospun nanofibers as drug delivery systems
- •3.3.1 Blending electrospinning
- •3.3.2 Emulsion electrospinning
- •3.3.3 Coaxial electrospinning
- •3.3.4 Surface modifications
- •3.4 Electrospun nanofibers for tissue engineering
- •3.4.1 Electrospun nanofibers for hard tissue engineering
- •3.5 Cancer diagnosis and therapy
- •3.6 Concluding remarks and future perspectives
- •Keywords
- •References
- •4. Natural Biocarriers for Brain Targeting
- •Abstract
- •4.1 Introduction
- •4.1.1 Central nervous system
- •4.2 Biocarriers
- •4.2.1 Carbohydrates carriers
- •4.2.2 Protein carriers
- •4.2.3 Exosomes
- •4.3 Conclusions and perspectives
- •Keywords
- •References
- •Abstract
- •5.1 Introduction
- •5.2 Synthesis of graphene family nanomaterials
- •5.2.1 Graphene synthesis
- •5.2.2 GO and rGO Syntheses
- •5.2.3 GQd synthesis
- •5.4 Drug delivery and biomedical applications
- •5.4.1 Drug delivery
- •5.4.2 Gene delivery
- •5.4.3 Bioimaging
- •5.4.4 Photothermal therapy
- •5.4.5 Tissue engineering
- •5.5 Summary and future prospect
- •Keywords
- •References
- •6. Nanotechnology in Gene Delivery
- •Abstract
- •6.1 Introduction
- •6.2 Gene delivery
- •6.3 Nanotechnology in gene delivery
- •Keywords
- •References
- •Abstract
- •7.1 Introduction
- •7.2 Additive manufacturing in pharmacology
- •7.2.1 Extrusion-based 3D printing techniques
- •7.2.2 Stereolithography
- •7.2.3 Selective laser sintering
- •7.2.4 Binder jet printing
- •7.3 Most common polymers
- •7.3.1 Natural polymers
- •7.3.2 Synthetic polymers
- •7.3.2.5 Polyvinylpyrrolidone
- •7.4 Common 3D-printed dosage forms
- •7.4.1 Scaffolds
- •7.4.2 Tablets
- •Keywords
- •References
- •7.4.3 Microneedles
- •7.4.4 Capsule
- •7.4.5 Films
- •7.5 Main factors in drug delivery
- •7.5.1 Nature of polymers
- •7.5.2 Matrix permeability
- •7.5.3 Polymer blends
- •7.5.4 Specific surface area
- •7.5.5 Infill density and patterns
- •7.5.6 Pores
- •7.5.7 Cross-linking
- •7.5.8 Coating
- •7.5.9 Core/shell and multicompartment
- •7.6 Final considerations and future perspectives
- •Abstract
- •8.1 Introduction
- •8.2.1 Polymer solution concentration and viscosity
- •8.2.2 Molecular weight of polymer
- •8.2.3 Surface tension
- •8.2.4 Electrical conductivity
- •8.2.5 Applied voltage
- •8.2.6 Feed rate/flow rate
- •8.2.7 Temperature and humidity
- •8.3 Method of preparation for nanofibers
- •8.3.1 Electrospinning
- •8.3.2 Self-assembly
- •8.3.3 Phase separation
- •8.3.4 Drawing of nanofibers
- •8.3.5 Template synthesis
- •8.4 Biomedical applications of nanofibers
- •8.4.1 Wound dressing
- •8.4.2 Tissue engineering
- •8.4.3 In cancer therapy
- •8.4.4 Miscellaneous
- •8.5 Drug delivery application
- •8.5.1 Antihypertensive drug
- •8.5.2 Antimicrobial drug
- •8.5.3 Growth hormone
- •8.5.4 Miscellaneous
- •8.6 Conclusion
- •Keywords
- •References
- •Abstract
- •9.1 Introduction
- •9.2 Tissue engineering
- •9.3 Nanotechnology
- •9.4 Polymeric scaffolds in tissue engineering
- •9.5 Challenges
- •Keywords
- •References
- •Abstract
- •10.1 Introduction
- •10.2 Ideal properties of bioceramics
- •10.2.1 Mechanical property
- •10.2.2 Porosity, pore size, and shape
- •10.2.3 Biocompatibility and biodegradability
- •10.2.4 Osteoconductivity and osseointegrity
- •10.3 Bioceramics in orthopedic applications
- •10.4 Bioceramics in maxillofacial surgery
- •10.5 Bioceramic in drug delivery applications
- •10.6 Doped bioceramic in biomedical application
- •10.7 Conclusions
- •10.8 Future direction
- •Acknowledgments
- •Keywords
- •References
- •Index

278
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
9.3 NANOTECHNOLOGY
the imagination, as it is an area that encompasses structures that present only
. Nanotechnology is directly
various pathologies (Haris et al., 2023).
drugs, materials, medical tools, and also analysis equipment. Since antimi-
crobial materials are nanotechnological materials applied to the health sector
nanoparticles can be incorporated into medical products, applied to the metal
, nanotechnology has contributed immensely to the

Nanotechnology-based Polymeric Scaffolds in Tissue Engineering
279
, as they play a unique role in tissue regeneration
(Fernandes et al., 2021).
, such as more outstanding adhesion and cell
-
areas (Langer and Vacanti, 2016). Within this context, due to the micro and
nanoscale inherent in biological processes, the composition, and the need to
-
Dong et al., 2020).
is the scale at
are essential in this area, as they can act directly on trauma and patholo-

280
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
-
-
containing internal bleeding sites (Hasan et al., 2018).
health area.
9.4 POLYMERIC SCAFFOLDS IN TISSUE ENGINEERING
-
out both by the ancient Egyptians and in the Roman Empire. With the
use (Dolcimascolo et al., 2019).

Nanotechnology-based Polymeric Scaffolds in Tissue Engineering
281
roughness, charge, reactivity, hydrophilicity, and rigidity. In this aspect, the
-
.-
et al., 2014).
-
.
.,
et al., 2017).
synthetic polymers, ceramics, metals, composites, and hydrogels are being

282
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
(i) biocompatibility, (ii) bioactivity, and (iii) biodegradability.
collagen, to produce a biomimetic environment equivalent to the native
-
Hutmacher, 2000).
-

Nanotechnology-based Polymeric Scaffolds in Tissue Engineering
283
-
tissue-based materials commonly present in nature, as they exist in various
et al., 2010) and collagen (Shen et
al.
.
heterogeneity , high dispersion, biocompatibility, less toxicity, and metabolic
(Ebhodaghe, 2021).
-
Biopolymers are polymers produced by living organisms, such as micro-
(Stoppel et al., 2015). In this respect, biopolymers can be an alternative to
In addition, some nondegradable polymers such as poly(acrylic acid) (PAA)
and its derivatives [such as poly(2-hydroxyethyl methacrylate) (PHEMA)]
body (Hollander et al.

284
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
-
-
these polymers can be disadvantageous in tissue regeneration applications
-
al., et al2002).
9.5 CHALLENGES
-
standing and assisting in constructing models that are more like the tissue to
-

Nanotechnology-based Polymeric Scaffolds in Tissue Engineering
285
maintain, regenerate, or replace tissues or organs.
KEYWORDS
• nanotechnology
• polymeric scaffolds
• tissue engineering
• biomaterials
• extracellular matrix
• cell adhesion
• porosity
REFERENCES
Tissue Engineering Made Easy
vol 1, pp 3–16.
Open-Source Fused Deposition Modeling. Emerg. Mater. 2020, 3 (4), 429–439.
Biomacromolecules 2003, 4 (6), 1466–1486.
Structural Biotechnology Analytical Methods. Comput. Struct. Biotechnol. J. 2019, 17,
591–598.

286
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
and Application to Human Embryonic Stem Cells. Nat. Biotechnol. 2004, 22 (7), 863–866.
engineered devices. Adv. Drug Deliv. Rev. 1998, 33 (1–2), 111–139.
Mater . Sci. Eng.: C 2020,
110, 110698–1107728.
Pharmaceutics 2022, 14, 1127–1153.
Mater. Today: Proc.
2021, 41, 397–402.
Int. J. Polym. Sci. 2012, 2012, 1–25.
Regenerative medicine and Tissue Engineering-cells and Biomaterials,
et al.
Biomaterials 2010, 31
(36), 9438–9451.
et al.
Stem
Cells 2014, 32 (1), 35–44.
Biomaterial-Supported Tissue Reconstruction or Regeneration,
IntechOpen, 2019.
Biomaterials 2020, 229, 119584–119604.
J.
Biomater. Sci. Polym. Ed. 2021, 32 (16), 2144–2194.
Int. J. Polym. Mater. Polym. Biomater. 2022, 71 (3), 155–172.
Wound Healing. Mater. Today Chem. 2022, 23, 100670–100685.
Front. Bioeng. Biotechnol. 2019, 7, 1–22.
Nanoengineering of Biomaterials – Volume II: Biomedical
Applications
J. Biomed. Mater. Res. 1983, 17 (3),
539–555.
Synthetic Polymers. Biotechnol. Ann. Rev. 2006, 12, 301–347.

Nanotechnology-based Polymeric Scaffolds in Tissue Engineering
287
Production and its Development. Sci. Total Environ. 2023, 857, 159639–159657.
Int. J. Nanomed. 2018, 13,
5637–5655.
et al.
Macromol. Biosci. 2007, 7, 23–39.
Biomaterials 2000,
21 (24), 2529–2543.
Et al.
J. Tissue
Eng, Regenerat. Med. 2007, 1 (4), 245–260.
et al.
J. Biomed. Mater. Res. Part B: Appl. Biomater 2017,
105 (2), 431–459.
Nanoengineering of Biomaterials: Drug Delivery & Biomedical Applications.
2022, p 3527349049.
Nat.
Rev. Mater. 2020, 5 (8), 584–603.
Applications. Nanomaterials 2020, 10, 1–60.
J. Pediatr. Surg. 2016, 51, 8–12.
Tissue Eng. 1993, 98.
et al.
Applications. Tissue Eng. 1995, 1(2), 151–161.
Principles of Tissue Engineering
Press, 2020, p 0128214015.
.
Adv. Healthc. Mater. 2014, 3 (4), 469–484.
et al.
Nat. Rev. Rheumatol. 2015, 11 (1), 21–34.
et al.
Acta Biomater.
2010, 6 (11), 4208–4217.
World J. Stem Cell. 2015, 7 (3),
657.
Bio. Mater. 2019, 4, 271–292.
J. Appl. Biotechnol. Rep. 2018, 5
(3), 81–91.
3D Bioprinting and Nanotechnology in Tissue Engineering and
Соседние файлы в папке Библиотека им академика М.И. Перельмана
