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_5705_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

288
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
Regenerative Medicine
3–32.
Int. J. Emerg. Technol. Adv. Eng. 2012, 2 (4), 91–101.
tissue engineering. Chemical Society Reviews 2009, 38 (4), 1139–1151.
Polym. Rev. 2008, 48 (1), 11–63.
Polymers 2021, 13 (7), 1105.
Int. J. Biol.
Macromol. 2013, 62, 465–471.
et al.
Biomaterials 2014, 35 (28), 8154–8163.
Smart Mater. Manufact. 2023,
1, 100011–100027.
Annal. Biomed.
Eng. 2015, 43 (3), 657–680.
J. R. Soc. Interface
2009, 6
Adv. Sci. 2019, 6, 1801664–1801711.
Adv.
Healthc. Mater. 2018, 7, 1701503–1701513.
J. Funct. Biomater. 2018, 9 (1), 17.
Adv. Exp. Med. Biol. 2022, 1–28.
Materials. Surf. Sci. 2002, 500 (1–3), 61–83.
et al.
J. Pediatr. Surg. 1988, 23 (1), 3–9.
Current Status and Challenges 2022, 193–236.
J. Biomed. Mater. Res. Part B Appl. Mater. 2022, 110, 1206–1214.
Handbook of Nanostructured Biomaterials and Their Applications in Nanobiotechnology
2005, 1, 1–23.

Nanotechnology-based Polymeric Scaffolds in Tissue Engineering
289
et al.
Skin Fibroblast Cell Culture. J. Biomed. Mater. Res. 2002, 62 (3), 438–446.
et al.
Mater. Lett. 2013, 93, 133–136.
Engineering. Adv. Healthc. Mater. 2015, 4 (9), 1268–1285.
et al.
Emerg. Mater.
2019, 2 (2), 141–151.


Advances in Pharmaceutical T echnology for Drug Delivery Systems (PTDDS), Volume 2: Recent Progress
in Biomedical Applications. Sougata Jana (Ed.)
© 2025 Apple Academic Press, Inc. Co-published with CRC Press (Taylor & Francis)
Bioceramics System for Biomedical
Application
V. LALZAWMLIANA
1
, PRASENJIT MUKHERJEE
2
, SUBHASIS ROY
2
,
SHUBHAMITRA CHAUDHURI
2
, and SAMIT KUMAR NANDI
3
1
2
3
CHAPTER 10
ABSTRACT
-
-
approaches such as orthopedic surgery, drug delivery systems, dental
discuss recent advancements in bioceramics systems and their application
in biomedical sciences.

292
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
10.1 INTRODUCTION
-
(titanium or tantalum), polymers (polylactides), hydrogel-based mate-
rials, bioceramics, biocomposite structures, etc. (Bohner et al., 2012).
various biomedical applications such as hip and knee replacement, and
(Saini et al., 2015).

Bioceramics System for Biomedical Application
293
-
-
-
materials are mostly bioactive and bioresorbable ceramics, such as calcium
should degrade at the same rate as the tissue regeneration and excrete

294
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
10.2 IDEAL PROPERTIES OF BIOCERAMICS
usually 3D structures to provide mechanical support and also promote the
-
causing any adverse reaction to the body . In addition to its acceptance by the
10.2.1 MECHANICAL PROPERTY
-
optimum in vivo
completely regenerated (Hollinger and Chaudhari, 1992). Additionally, the
ceramic material must possess other properties such as optimum elasticity,
-

Bioceramics System for Biomedical Application
295
-
2015).
10.2.2 POROSITY, PORE SIZE, AND SHAPE
-

296
Advances in Pharmaceutical Technology for Drug Delivery Systems (PTDDS), Volume 2
-
bone healing. A larger interconnected pore structure can be attained by rapid
-
(Leong et al., 2003).
10.2.3 BIOCOMPATIBILITY AND BIODEGRADABILITY
-
be nontoxic, nonteratogenic, noncarcinogenic, nonallergic, nonhemolytic,
-

Bioceramics System for Biomedical Application
297
bioresorbable properties (Bohner, 2000).
10.2.4 OSTEOCONDUCTIVITY AND OSSEOINTEGRITY
-
and biodegradability (Li et al., 2021). Besides, osteointegration means the
-
-
Соседние файлы в папке Библиотека им академика М.И. Перельмана
