Abstract
Despite recent advances in drug delivery systems and tissue engineering, several challenges still need to be overcome for these new technologies to reach patients. The number of new cancer cases is increasing yearly, and the future projection is frightening. Another major health concern is the rise of antibiotic-resistant bacteria. The uncontrolled and excessive use of antibiotics has allowed bacteria to undergo mutation processes, decreasing the efficiency of this sort of drug. Therefore, the development of new medical devices is a battle against time to prevent projections on the advancement of diseases from being reached. Given this scenario, redox-sensitive and temperature-sensitive drug delivery platforms show promising results in the release of bioactive molecules. This review covers the most recent advances involving devices obtained from inorganic and polymeric matrices and their structuring as scaffolds and 3D printing, focusing on their potentiality of redox and temperature sensitivity for biomedical applications.
Graphical Abstract
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Data Availability
All data are provided with paper.
Abbreviations
- AMF:
-
Alternating magnetic field
- DOX:
-
Doxorubicin
- FRET:
-
Fluorescence resonance energy transfer
- GSH:
-
Glutathione
- LCST:
-
Lower critical solubility temperature
- MFH:
-
Fluid hyperthermia
- MOFs:
-
Metal–organic frameworks
- MRI:
-
Magnetic resonance imaging
- MWCNTs:
-
Multi-walled carbon nanotubes
- NIR:
-
Near-infrared
- NPs:
-
Nanoparticles
- PCL:
-
Polycaprolactam
- PDT:
-
Photodynamic therapy
- PEG:
-
Polyethyleneglycol
- PNIPAAm:
-
Poly(isopropylacrylamide)
- PTT:
-
Photothermal therapy
- PVCL:
-
Polyvinyl caprolactam
- QDs:
-
Quantum dots
- ROS:
-
Reactive oxygen species
- SPION:
-
Superparamagnetic iron oxide nanoparticles
References
M. Saeedi, M. Eslamifar, K. Khezri, S.M. Dizaj, Applications of nanotechnology in drug delivery to the central nervous system. Biomed. Pharmacother. 111, 666–675 (2019). https://doi.org/10.1016/J.BIOPHA.2018.12.133
N. Zahin, R. Anwar, D. Tewari et al., Nanoparticles and its biomedical applications in health and diseases: special focus on drug delivery. Environ. Sci. Pollut. Res. 27, 19151–19168 (2020). https://doi.org/10.1007/s11356-019-05211-0
A. Radaic, M.B. de Jesus, Y.L. Kapila, Bacterial anti-microbial peptides and nano-sized drug delivery systems: the state of the art toward improved bacteriocins. J. Control. Release 321, 100–118 (2020). https://doi.org/10.1016/J.JCONREL.2020.02.001
K. Dua, R. Wadhwa, G. Singhvi et al., The potential of siRNA based drug delivery in respiratory disorders: recent advances and progress. Drug Dev. Res. 80, 714–730 (2019). https://doi.org/10.1002/DDR.21571
ORGANIZATION WH, World health statistics 2018: monitoring health for the SDGs, sustainable development goals (2018), https://www.who.int/gho/publications/world_health_statistics/en/. Accessed 22 May 2019
K.R. Yabroff, A. Mariotto, F. Tangka et al., Annual Report to the Nation on the Status of Cancer, Part 2: patient economic burden associated with cancer care. J. Natl. Cancer Inst. 113, 1670–1682 (2021). https://doi.org/10.1093/JNCI/DJAB192
European Medicines Agency, European Medicines Agency - Antimicrobial resistance (2015), https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/antimicrobial-resistance. Accessed 28 Sep 2021
R. Canaparo, F. Foglietta, F. Giuntini et al., Recent developments in antibacterial therapy: focus on stimuli-responsive drug-delivery systems and therapeutic nanoparticles. Molecules 24, 1991 (2019). https://doi.org/10.3390/molecules24101991
F. Laffleur, V. Keckeis, Advances in drug delivery systems: work in progress still needed? Int. J. Pharm. 590, 119912 (2020). https://doi.org/10.1016/J.IJPHARM.2020.119912
K. Park, Controlled drug delivery systems: past forward and future back. J. Control Release 190, 3–8 (2014). https://doi.org/10.1016/j.jconrel.2014.03.054
W. Lu, J. Yao, X. Zhu, Y. Qi, Nanomedicines: redefining traditional medicine. Biomed. Pharmacother. 134, 111103 (2021). https://doi.org/10.1016/j.biopha.2020.111103
W.W. Gan, L.W. Chan, W. Li, T.W. Wong, Critical clinical gaps in cancer precision nanomedicine development. J. Control. Release 345, 811–818 (2022). https://doi.org/10.1016/J.JCONREL.2022.03.055
R.A. Siegel, Stimuli sensitive polymers and self regulated drug delivery systems: a very partial review. J. Control. Release 190, 337–351 (2014). https://doi.org/10.1016/j.jconrel.2014.06.035
E. Issaka, M.A. Wariboko et al., Synergy and coordination between biomimetic nanoparticles and biological cells/tissues/organs/systems: applications in nanomedicine and prospect. Biomed. Mater. Dev. 1, 1–33 (2023). https://doi.org/10.1007/S44174-023-00084-X
E. Fleige, M.A. Quadir, R. Haag, Stimuli-responsive polymeric nanocarriers for the controlled transport of active compounds: concepts and applications. Adv. Drug Deliv. Rev. 64, 866–884 (2012). https://doi.org/10.1016/j.addr.2012.01.020
Q. Sun, Z. Wang, B. Liu et al., Recent advances on endogenous/exogenous stimuli-triggered nanoplatforms for enhanced chemodynamic therapy. Coord. Chem. Rev. (2022). https://doi.org/10.1016/J.CCR.2021.214267
J.L. Zhang, R.S. Srivastava, R.D.K. Misra, Core−shell magnetite nanoparticles surface encapsulated with smart stimuli-responsive polymer: synthesis, characterization, and LCST of viable drug-targeting delivery system. Langmuir 23, 6342–6351 (2007). https://doi.org/10.1021/la0636199
J. Zhang, R.D.K. Misra, Magnetic drug-targeting carrier encapsulated with thermosensitive smart polymer: core–shell nanoparticle carrier and drug release response. Acta Biomater. 3, 838–850 (2007). https://doi.org/10.1016/J.ACTBIO.2007.05.011
R. Cheng, F. Meng, C. Deng et al., Dual and multi-stimuli responsive polymeric nanoparticles for programmed site-specific drug delivery. Biomaterials 34, 3647–3657 (2013). https://doi.org/10.1016/J.BIOMATERIALS.2013.01.084
L. Wei, C. Cai, J. Lin, T. Chen, Dual-drug delivery system based on hydrogel/micelle composites. Biomaterials 30, 2606–2613 (2009). https://doi.org/10.1016/j.biomaterials.2009.01.006
K. Numata, S. Yamazaki, N. Naga, Biocompatible and biodegradable dual-drug release system based on silk hydrogel containing silk nanoparticles. Biomacromol 13, 1383–1389 (2012). https://doi.org/10.1021/bm300089a
S. Aryal, C.M.J. Hu, L. Zhang, Combinatorial drug conjugation enables nanoparticle dual-drug delivery. Small 6, 1442–1448 (2010). https://doi.org/10.1002/smll.201000631
S. Yan, L. Xiaoqiang, L. Shuiping et al., Controlled release of dual drugs from emulsion electrospun nanofibrous mats. Colloids Surf. B 73, 376–381 (2009). https://doi.org/10.1016/j.colsurfb.2009.06.009
R.A. Bini, M.F. Silva, L.C. Varanda et al., Soft nanocomposites of gelatin and poly(3-hydroxybutyrate) nanoparticles for dual drug release. Colloids Surf. B 157, 191–198 (2017). https://doi.org/10.1016/J.COLSURFB.2017.05.051
Y. Zhang, Y. Feng, Stimuli-responsive microemulsions: state-of-the-art and future prospects. Curr. Opin. Colloid Interface Sci. 49, 27–41 (2020)
S.F. Medeiros, A.M. Santos, H. Fessi, A. Elaissari, Stimuli-responsive magnetic particles for biomedical applications. Int. J. Pharm. 403, 139–161 (2011). https://doi.org/10.1016/j.ijpharm.2010.10.011
M.C. Koetting, J.T. Peters, S.D. Steichen, N.A. Peppas, Stimulus-responsive hydrogels: theory, modern advances, and applications. Mater. Sci. Eng. R 93, 1–49 (2015). https://doi.org/10.1016/j.mser.2015.04.001
Y. Wang, F. Gao, X. Li et al., Tumor microenvironment-responsive fenton nanocatalysts for intensified anticancer treatment. J. Nanobiotechnol. 20, 69 (2022)
Q. Cui, J.Q. Wang, Y.G. Assaraf et al., Modulating ROS to overcome multidrug resistance in cancer. Drug Resist. Updates 41, 1–25 (2018). https://doi.org/10.1016/J.DRUP.2018.11.001
D.J. Dietzen, Amino acids, peptides, and proteins, in Principles and Applications of Molecular Diagnostics (Elsevier, 2018), pp. 345–380
E. Desideri, F. Ciccarone, M.R. Ciriolo, Targeting glutathione metabolism: partner in crime in anticancer therapy. Nutrients 11, 1926 (2019). https://doi.org/10.3390/nu11081926
L. Brülisauer, M.A. Gauthier, J. Leroux, Disulfide-containing parenteral delivery systems and their redox-biological fate. J. Control. Release (2014). https://doi.org/10.1016/j.jconrel.2014.06.012
M. Alsehli, Polymeric nanocarriers as stimuli-responsive systems for targeted tumor (cancer) therapy: recent advances in drug delivery. Saudi Pharm. J. 28, 255–265 (2020). https://doi.org/10.1016/j.jsps.2020.01.004
C. Forni, M. Rossi, I. Borromeo et al., Flavonoids: a myth or a reality for cancer therapy? Molecules 26, 3583 (2021). https://doi.org/10.3390/molecules26123583
J.J. Lim, S. Grinstein, Z. Roth, Diversity and versatility of phagocytosis: roles in innate immunity, tissue remodeling, and homeostasis. Front. Cell. Infect. Microbiol. 7, 191 (2017). https://doi.org/10.3389/fcimb.2017.00191
A.T. Dharmaraja, Role of Reactive Oxygen Species (ROS) in therapeutics and drug resistance in cancer and bacteria. J. Med. Chem. 60, 3221–3240 (2017). https://doi.org/10.1021/ACS.JMEDCHEM.6B01243
P.F. Monteiro, A. Travanut, C. Conte, C. Alexander, Reduction-responsive polymers for drug delivery in cancer therapy—is there anything new to discover? Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. (2021). https://doi.org/10.1002/WNAN.1678
V.G. Deepagan, S. Kwon, D.G. You et al., In situ diselenide-crosslinked polymeric micelles for ROS-mediated anticancer drug delivery. Biomaterials 103, 56–66 (2016). https://doi.org/10.1016/j.biomaterials.2016.06.044
N. Ma, Y. Li, H. Xu et al., Dual redox responsive assemblies formed from diselenide block copolymers. J. Am. Chem. Soc. 132, 442–443 (2010). https://doi.org/10.1021/ja908124g
E.A. Repasky, S.S. Evans, M.W. Dewhirst, Temperature matters! and why it should matter to tumor immunologists. Cancer Immunol. Res. 1, 210 (2013). https://doi.org/10.1158/2326-6066.CIR-13-0118
J. Miner, A. Hoffhines, The discovery of aspirin’s antithrombotic effects. Tex Heart Inst. J. 34, 179–186 (2007)
S. Wrotek, E.K. LeGrand, A. Dzialuk, J. Alcock, Let fever do its job. Evol. Med. Public Health 9, 26–35 (2021). https://doi.org/10.1093/emph/eoaa044
J.J. González Plaza, N. Hulak, Z. Zhumadilov, A. Akilzhanova, Fever as an important resource for infectious diseases research. Intractable Rare Dis. Res. 5, 97–102 (2016). https://doi.org/10.5582/irdr.2016.01009
M.T. Cook, P. Haddow, S.B. Kirton, W.J. McAuley, Polymers Exhibiting lower critical solution temperatures as a route to thermoreversible gelators for healthcare. Adv. Funct. Mater. 31, 2008123 (2021). https://doi.org/10.1002/adfm.202008123
Q. Zhang, S. Dong, M. Zhang, F. Huang, Supramolecular control over thermo-responsive systems with lower critical solution temperature behavior. Aggregate 2, 35–47 (2021). https://doi.org/10.1002/agt2.12
W. Xiong, W. Wang, Y. Wang et al., Dual temperature/pH-sensitive drug delivery of poly(N-isopropylacrylamide-co-acrylic acid) nanogels conjugated with doxorubicin for potential application in tumor hyperthermia therapy. Colloids Surf. B 84, 447–453 (2011). https://doi.org/10.1016/j.colsurfb.2011.01.040
B.E. Amantea, R.D. Piazza, J.R.V. Chacon et al., Esterification influence in thermosensitive behavior of copolymers PNIPAm-co-PAA and PNVCL-co-PAA in magnetic nanoparticles surface. Colloids Surf. A 575, 18–26 (2019). https://doi.org/10.1016/J.COLSURFA.2019.04.011
R.D. Piazza, W.R. Viali, C.C. dos Santos et al., PEGlatyon-SPION surface functionalization with folic acid for magnetic hyperthermia applications. Mater. Res. Express (2020). https://doi.org/10.1088/2053-1591/ab6700
G.N. Lucena, C.C. dos Santos, G.C. Pinto, et al., Drug delivery and magnetic hyperthermia based on surface engineering of magnetic nanoparticles, in Magnetic Nanoparticles in Human Health and Medicine, ed. by C. Caizer, M. Rai (Wiley, 2021), pp. 231–249
G. Eskiizmir, A.T. Ermertcan, K. Yapici, Nanomaterials: promising structures for the management of oral cancer, in Nanostructures for Oral Medicine (Elsevier, 2017), pp. 511–544
J.R. Melamed, R.S. Edelstein, E.S. Day, Elucidating the fundamental mechanisms of cell death triggered by photothermal therapy. ACS Nano 9, 6–11 (2015). https://doi.org/10.1021/ACSNANO.5B00021
P.K. Jain, X. Huang, I.H. El-Sayed, M.A. El-Sayed, Noble metals on the nanoscale: optical and photothermal properties and some applications in imaging, sensing, biology, and medicine. Acc. Chem. Res. 41, 1578–1586 (2008). https://doi.org/10.1021/ar7002804
J.B. Vines, J.-H. Yoon, N.-E. Ryu et al., Gold nanoparticles for photothermal cancer therapy. Front. Chem. (2019). https://doi.org/10.3389/fchem.2019.00167
H. Kang, J.T. Buchman, R.S. Rodriguez et al., Stabilization of silver and gold nanoparticles: preservation and improvement of plasmonic functionalities. Chem. Rev. 119, 664–699 (2019). https://doi.org/10.1021/acs.chemrev.8b00341
M. Rycenga, C.M. Cobley, J. Zeng et al., Controlling the synthesis and assembly of silver nanostructures for plasmonic applications. Chem. Rev. 111, 3669–3712 (2011). https://doi.org/10.1021/cr100275d
S. Eckhardt, P.S. Brunetto, J. Gagnon et al., Nanobio silver: its interactions with peptides and bacteria, and its uses in medicine. Chem. Rev. 113, 4708–4754 (2013). https://doi.org/10.1021/cr300288v
M.-C. Daniel, D. Astruc, Gold nanoparticles: assembly, supramolecular chemistry, quantum-size-related properties, and applications toward biology, catalysis, and nanotechnology. Chem. Rev. 104, 293–346 (2004). https://doi.org/10.1021/CR030698
C.M. Cobley, L. Au, J. Chen, Y. Xia, Targeting gold nanocages to cancer cells for photothermal destruction and drug delivery. Expert Opin. Drug Deliv. 7, 577–587 (2010). https://doi.org/10.1517/17425240903571614
Y. Yang, Q. Zhang, M. Cai et al., Size-dependent transmembrane transport of gold nanocages. ACS Omega 5, 9864–9869 (2020). https://doi.org/10.1021/acsomega.0c00079
J. Wang, A.M. Potocny, J. Rosenthal, E.S. Day, Gold nanoshell-linear tetrapyrrole conjugates for near infrared-activated dual photodynamic and photothermal therapies. ACS Omega 5, 926–940 (2020). https://doi.org/10.1021/acsomega.9b04150
M.L. Ermini, V. Voliani, Antimicrobial nano-agents: the copper age. ACS Nano 15, 6008–6029 (2021)
R. Giampietro, F. Spinelli, M. Contino, N.A. Colabufo, The pivotal role of copper in neurodegeneration: a new strategy for the therapy of neurodegenerative disorders. Mol. Pharm. 15, 808–820 (2018)
V. Kumar, A. Kumar, N.S. Chauhan et al., Design and fabrication of a dual protein-based trilayered nanofibrous scaffold for efficient wound healing. ACS Appl. Bio Mater. 5, 2726–2740 (2022). https://doi.org/10.1021/acsabm.2c00200
I. Jahan, E. George, N. Saxena, S. Sen, Silver-nanoparticle-entrapped soft GelMA gels as prospective scaffolds for wound healing. ACS Appl. Bio Mater. 2, 1802–1814 (2019). https://doi.org/10.1021/acsabm.8b00663
J. Xiao, Y. Zhu, S. Huddleston et al., Copper metal-organic framework nanoparticles stabilized with folic acid improve wound healing in diabetes. ACS Nano 12, 1023–1032 (2018). https://doi.org/10.1021/acsnano.7b01850
J. Qian, L. Ji, W. Xu et al., Copper-hydrazide coordinated multifunctional hyaluronan hydrogels for infected wound healing. ACS Appl. Mater. Interfaces 14, 16018–16031 (2022). https://doi.org/10.1021/acsami.2c01254
D. Bobo, K.J. Robinson, J. Islam et al., Nanoparticle-based medicines: a review of FDA-approved materials and clinical trials to date. Pharm. Res. 33, 2373–2387 (2016)
M. Nabavinia, J. Beltran-Huarac, Recent progress in iron oxide nanoparticles as therapeutic magnetic agents for cancer treatment and tissue engineering. ACS Appl. Bio Mater. 3, 8172–8187 (2020). https://doi.org/10.1021/acsabm.0c00947
S. Khizar, N.M. Ahmad, N. Zine et al., Magnetic nanoparticles: from synthesis to theranostic applications. ACS Appl. Nano Mater. 4, 4284–4306 (2021). https://doi.org/10.1021/acsanm.1c00852
L. Arias, J. Pessan, A. Vieira et al., Iron oxide nanoparticles for biomedical applications: a perspective on synthesis, drugs, antimicrobial activity, and toxicity. Antibiotics 7, 46 (2018). https://doi.org/10.3390/antibiotics7020046
Q. Zhao, P. Xie, X. Li et al., Magnetic mesoporous silica nanoparticles mediated redox and pH dual-responsive target drug delivery for combined magnetothermal therapy and chemotherapy. Colloids Surf. A (2022). https://doi.org/10.1016/j.colsurfa.2022.129359
G. Birlik Demirel, Ş Bayrak, Ultrasound/redox/pH-responsive hybrid nanoparticles for triple-triggered drug delivery. J. Drug Deliv. Sci. Technol. (2022). https://doi.org/10.1016/j.jddst.2022.103267
Y. Li, X. Ma, X. Liu et al., Redox-responsive functional iron oxide nanocrystals for magnetic resonance imaging-guided tumor hyperthermia therapy and heat-mediated immune activation. ACS Appl. Nano Mater. 5, 4537–4549 (2022). https://doi.org/10.1021/acsanm.2c00898
L. Zhang, Y. Li, J.C. Yu, Chemical modification of inorganic nanostructures for targeted and controlled drug delivery in cancer treatment. J. Mater. Chem. B 2, 452–470 (2014). https://doi.org/10.1039/c3tb21196g
E. Bagheri, L. Ansari, K. Abnous et al., Silica based hybrid materials for drug delivery and bioimaging. J. Control. Release 277, 57–76 (2018). https://doi.org/10.1016/j.jconrel.2018.03.014
N. Yin, X. Wang, T. Yang et al., Multifunctional Fe3O4 cluster@ quantum dot-embedded mesoporous SiO2 nanoplatform probe for cancer cell fluorescence-labelling detection and photothermal therapy. Ceram. Int. 47, 8271–8278 (2021). https://doi.org/10.1016/j.ceramint.2020.11.188
M.J. Molaei, E. Salimi, Magneto-fluorescent superparamagnetic Fe3O4@SiO2@alginate/carbon quantum dots nanohybrid for drug delivery. Mater. Chem. Phys. (2022). https://doi.org/10.1016/j.matchemphys.2022.126361
X. Su, C. Chan, J. Shi et al., A graphene quantum dot@Fe3O4@SiO2 based nanoprobe for drug delivery sensing and dual-modal fluorescence and MRI imaging in cancer cells. Biosens. Bioelectron. 92, 489–495 (2017). https://doi.org/10.1016/j.bios.2016.10.076
S. Su, L. Lin, H. Li et al., Preparation and properties study of F-SiO2@MPDA-AuNPs drug nanocarriers. Microporous Mesoporous Mater. (2022). https://doi.org/10.1016/j.micromeso.2021.111571
Z. Gao, T. Shi, Y. Li et al., Mesoporous silica-coated gold nanoframes as drug delivery system for remotely controllable chemo-photothermal combination therapy. Colloids Surf. B 176, 230–238 (2019). https://doi.org/10.1016/j.colsurfb.2019.01.005
C. Veeramani, A.S.E. Newehy, M.A. Alsaif, K.S. Al-Numair, Pouteria Caimito nutritional fruit derived silver nanoparticles and core-shell nanospheres synthesis, characterization, and their oral cancer preventive efficiency. J. Mol. Struct. (2021). https://doi.org/10.1016/j.molstruc.2021.131227
S. Tamta, A. Dahiya, P.S. Kumar, Modified Stöber synthesis of SiO2@Ag nanocomposites and their enhanced refractive index sensing applications. Physica B (2022). https://doi.org/10.1016/j.physb.2022.413971
F. Lv, L. Fu, E.P. Giannelis, G. Qi, Preparation of γ-Fe2O3/SiO2-capsule composites capable of using as drug delivery and magnetic targeting system from hydrophobic iron acetylacetonate and hydrophilic SiO2-capsule. Solid State Sci 34, 49–55 (2014). https://doi.org/10.1016/j.solidstatesciences.2014.05.006
C.Y. Lai, B.G. Trewyn, D.M. Jeftinija et al., A mesoporous silica nanosphere-based carrier system with chemically removable CdS nanoparticle caps for stimuli-responsive controlled release of neurotransmitters and drug molecules. J. Am. Chem. Soc. 125, 4451–4459 (2003). https://doi.org/10.1021/ja028650l
J. Lai, B.P. Shah, E. Garfunkel, K.B. Lee, Versatile fluorescence resonance energy transfer-based mesoporous silica nanoparticles for real-time monitoring of drug release. ACS Nano 7, 2741–2750 (2013). https://doi.org/10.1021/nn400199t
J.T. Lin, J.K. Du, Y.Q. Yang et al., pH and redox dual stimulate-responsive nanocarriers based on hyaluronic acid coated mesoporous silica for targeted drug delivery. Mater. Sci. Eng. C 81, 478–484 (2017). https://doi.org/10.1016/j.msec.2017.08.036
M. Kundu, P. Sadhukhan, N. Ghosh et al., In vivo therapeutic evaluation of a novel bis-lawsone derivative against tumor following delivery using mesoporous silica nanoparticle based redox-responsive drug delivery system. Mater. Sci. Eng. C (2021). https://doi.org/10.1016/j.msec.2021.112142
S. Wang, A. Riedinger, H. Li et al., Plasmonic copper sulfide nanocrystals exhibiting near-infrared photothermal and photodynamic therapeutic effects. ACS Nano 9, 1788–1800 (2015). https://doi.org/10.1021/nn506687t
D. Mo, L. Hu, G. Zeng et al., Cadmium-containing quantum dots: properties, applications, and toxicity. Appl. Microbiol. Biotechnol. 101, 2713–2733 (2017). https://doi.org/10.1007/s00253-017-8140-9
A.M. Wagner, J.M. Knipe, G. Orive, N.A. Peppas, Quantum dots in biomedical applications. Acta Biomater. 94, 44–63 (2019). https://doi.org/10.1016/j.actbio.2019.05.022
K. Shivaji, S. Mani, P. Ponmurugan et al., Green-synthesis-derived CdS quantum dots using tea leaf extract: antimicrobial, bioimaging, and therapeutic applications in lung cancer cells. ACS Appl. Nano Mater. 1, 1683–1693 (2018). https://doi.org/10.1021/acsanm.8b00147
W.-H. Zhang, W. Ma, Y.-T. Long, Redox-mediated indirect fluorescence immunoassay for the detection of disease biomarkers using dopamine-functionalized quantum dots. Anal. Chem. 88, 5131–5136 (2016). https://doi.org/10.1021/acs.analchem.6b00048
N. Ma, A. Song, Z. Li, Y. Luan, Redox-sensitive prodrug molecules meet graphene oxide: an efficient graphene oxide-based nanovehicle toward cancer therapy. ACS Biomater. Sci. Eng. 5, 1384–1391 (2019). https://doi.org/10.1021/acsbiomaterials.9b00114
H. Chen, Z. Wang, S. Zong et al., SERS-fluorescence monitored drug release of a redox-responsive nanocarrier based on graphene oxide in tumor cells. ACS Appl. Mater. Interfaces 6, 17526–17533 (2014). https://doi.org/10.1021/am505160v
Z. Zhang, L. Hou, X. Yang et al., A novel redox-sensitive system based on single-walled carbon nanotubes for chemo-photothermal therapy and magnetic resonance imaging. Int. J. Nanomed. (2016). https://doi.org/10.2147/IJN.S98476
J. Jiao, C. Liu, X. Li et al., Fluorescent carbon dot modified mesoporous silica nanocarriers for redox-responsive controlled drug delivery and bioimaging. J. Colloid Interface Sci. 483, 343–352 (2016). https://doi.org/10.1016/j.jcis.2016.08.033
H.D. Lawson, S.P. Walton, C. Chan, Metal-organic frameworks for drug delivery: a design perspective. ACS Appl. Mater. Interfaces 13, 7004–7020 (2021). https://doi.org/10.1021/acsami.1c01089
Y. Li, S. Feng, P. Dai et al., Tailored Trojan horse nanocarriers for enhanced redox-responsive drug delivery. J. Control. Release 342, 201–209 (2022). https://doi.org/10.1016/j.jconrel.2022.01.006
X.-G. Wang, Z.-Y. Dong, H. Cheng et al., A multifunctional metal–organic framework based tumor targeting drug delivery system for cancer therapy. Nanoscale 7, 16061–16070 (2015). https://doi.org/10.1039/C5NR04045K
M. Xia, Y. Yan, H. Pu et al., Glutathione responsive nitric oxide release for enhanced photodynamic therapy by a porphyrinic MOF nanosystem. Chem. Eng. J. 442, 136295 (2022). https://doi.org/10.1016/j.cej.2022.136295
J. Tang, X. Zhang, L. Cheng et al., Multiple stimuli-responsive nanosystem for potent, ROS-amplifying, chemo-sonodynamic antitumor therapy. Bioact. Mater. 15, 355–371 (2022). https://doi.org/10.1016/j.bioactmat.2021.12.002
M. Wang, Y. Zhai, H. Ye et al., High co-loading capacity and stimuli-responsive release based on cascade reaction of self-destructive polymer for improved chemo-photodynamic therapy. ACS Nano 13, 7010–7023 (2019). https://doi.org/10.1021/acsnano.9b02096
G. Wang, P. Huang, M. Qi et al., Facile synthesis of a H2O2-responsive alternating copolymer bearing thioether side groups for drug delivery and controlled release. ACS Omega 4, 17600–17606 (2019). https://doi.org/10.1021/acsomega.9b02923
Z. Zhang, M. Yu, T. An et al., Tumor microenvironment stimuli-responsive polymeric prodrug micelles for improved cancer therapy. Pharm. Res. 37, 4 (2020). https://doi.org/10.1007/s11095-019-2709-1
S. Zafar Razzacki, Integrated microsystems for controlled drug delivery. Adv. Drug Deliv. Rev. 56, 185–198 (2004). https://doi.org/10.1016/j.addr.2003.08.012
K.F. Leong, C.K. Chua, W.S. Gui, Verani, Building porous biopolymeric microstructures for controlled drug delivery devices using selective laser sintering. Int. J. Adv. Manuf. Technol. 31, 483–489 (2006). https://doi.org/10.1007/s00170-005-0217-4
W.H. Ryu, M. Vyakarnam, R.S. Greco et al., Fabrication of multi-layered biodegradable drug delivery device based on micro-structuring of PLGA polymers. Biomed. Microdev. 9, 845–853 (2007). https://doi.org/10.1007/s10544-007-9097-8
J. Li, W. Fang, T. Hao et al., An anti-oxidative and conductive composite scaffold for cardiac tissue engineering. Composites B 199, 108285 (2020). https://doi.org/10.1016/j.compositesb.2020.108285
Y. Li, L. Yang, Y. Hou et al., Polydopamine-mediated graphene oxide and nanohydroxyapatite-incorporated conductive scaffold with an immunomodulatory ability accelerates periodontal bone regeneration in diabetes. Bioact. Mater. 18, 213–227 (2022). https://doi.org/10.1016/j.bioactmat.2022.03.021
C.-H. Mac, H.-Y. Chan, Y.-H. Lin et al., Engineering a biomimetic bone scaffold that can regulate redox homeostasis and promote osteogenesis to repair large bone defects. Biomaterials 286, 121574 (2022). https://doi.org/10.1016/j.biomaterials.2022.121574
B. Chen, J. Wang, X. Jin et al., Rapamycin incorporating hydrogel improves the progression of osteoarthritis by inducing synovial macrophages polarization and reducing intra-articular inflammation. Mater. Des. 225, 111542 (2023). https://doi.org/10.1016/j.matdes.2022.111542
Y. Xia, C. Li, J. Cao et al., Liposome-templated gold nanoparticles for precisely temperature-controlled photothermal therapy based on heat shock protein expression. Colloids Surf. B 217, 112686 (2022). https://doi.org/10.1016/j.colsurfb.2022.112686
J. Depciuch, M. Stec, A. Maximienko et al., Size-dependent theoretical and experimental photothermal conversion efficiency of spherical gold nanoparticles. Photodiagnosis Photodyn. Ther. 39, 102979 (2022). https://doi.org/10.1016/j.pdpdt.2022.102979
Y. Li, Y. Yan, J. Wang et al., Preparation of silver nanoparticles decorated mesoporous silica nanorods with photothermal antibacterial property. Colloids Surf. A (2022). https://doi.org/10.1016/j.colsurfa.2022.129242
D. Kim, R. Amatya, S. Hwang et al., BSA-silver nanoparticles: a potential multimodal therapeutics for conventional and photothermal treatment of skin cancer. Pharmaceutics 13, 575 (2021). https://doi.org/10.3390/pharmaceutics13040575
J. Wang, X. Zhao, F. Tang et al., Synthesis of copper nanoparticles with controllable crystallinity and their photothermal property. Colloids Surf. A 626, 126970 (2021). https://doi.org/10.1016/j.colsurfa.2021.126970
S. Naser Mohammed, A. Mishaal Mohammed, K.F. Al-Rawi, Novel combination of multi-walled carbon nanotubes and gold nanocomposite for photothermal therapy in human breast cancer model. Steroids 186, 109091 (2022). https://doi.org/10.1016/j.steroids.2022.109091
M.F. Naief, Y.H. Khalaf, A.M. Mohammed, Novel photothermal therapy using multi-walled carbon nanotubes and platinum nanocomposite for human prostate cancer PC3 cell line. J. Organomet. Chem. 975, 122422 (2022). https://doi.org/10.1016/j.jorganchem.2022.122422
X. Yan, J. Yang, J. Wu et al., Antibacterial carbon dots/iron oxychloride nanoplatform for chemodynamic and photothermal therapy. Colloid Interface Sci. Commun. 45, 100552 (2021). https://doi.org/10.1016/j.colcom.2021.100552
J. Wang, X. Zhao, F. Tang et al., Synthesis of copper nanoparticles with controllable crystallinity and their photothermal property. Colloids Surf. A (2021). https://doi.org/10.1016/j.colsurfa.2021.126970
A.F.R. Rodriguez, C.C. dos Santos, K. Lüdtke-Buzug et al., Evaluation of antiplasmodial activity and cytotoxicity assays of amino acids functionalized magnetite nanoparticles: hyperthermia and flow cytometry applications. Mater. Sci. Eng. C 125, 112097 (2021). https://doi.org/10.1016/j.msec.2021.112097
S.D. Fitzpatrick, L.E. Fitzpatrick, A. Thakur et al., Temperature-sensitive polymers for drug delivery. Expert Rev. Med. Dev. 9, 339–351 (2012). https://doi.org/10.1586/erd.12.24
Z. Liu, S. Zhang, B. He et al., Temperature-responsive hydroxypropyl methylcellulose-N-isopropylacrylamide aerogels for drug delivery systems. Cellulose 27, 9493–9504 (2020). https://doi.org/10.1007/s10570-020-03426-w
Z. Kou, D. Dou, H. Mo et al., Preparation and application of a polymer with pH/temperature-responsive targeting. Int. J. Biol. Macromol. 165, 995–1001 (2020). https://doi.org/10.1016/j.ijbiomac.2020.09.248
H. Long, W. Tian, S. Jiang et al., A dual drug delivery platform based on thermo-responsive polymeric micelle capped mesoporous silica nanoparticles for cancer therapy. Microporous Mesoporous Mater. 338, 111943 (2022). https://doi.org/10.1016/j.micromeso.2022.111943
R. Jahanban-Esfahlan, B. Massoumi, M. Abbasian et al., Dual stimuli-responsive polymeric hollow nanocapsules as “smart” drug delivery system against cancer. Polymer 59, 1492–1504 (2020). https://doi.org/10.1080/25740881.2020.1750652
X. Li, S. Bian, M. Zhao et al., Stimuli-responsive biphenyl-tripeptide supramolecular hydrogels as biomimetic extracellular matrix scaffolds for cartilage tissue engineering. Acta Biomater. 131, 128–137 (2021). https://doi.org/10.1016/j.actbio.2021.07.007
V. Santos-Rosales, B. Magariños, C. Alvarez-Lorenzo, C.A. García-González, Combined sterilization and fabrication of drug-loaded scaffolds using supercritical CO2 technology. Int. J. Pharm. (2022). https://doi.org/10.1016/j.ijpharm.2021.121362
X. Xu, Z. Gu, X. Chen et al., An injectable and thermosensitive hydrogel: promoting periodontal regeneration by controlled-release of aspirin and erythropoietin. Acta Biomater. 86, 235–246 (2019). https://doi.org/10.1016/j.actbio.2019.01.001
B. Wang, H.E. Booij-Vrieling, E.M. Bronkhorst et al., Antimicrobial and anti-inflammatory thermo-reversible hydrogel for periodontal delivery. Acta Biomater. 116, 259–267 (2020). https://doi.org/10.1016/j.actbio.2020.09.018
G.H. Yang, M. Yeo, Y.W. Koo, G.H. Kim, 4D bioprinting: technological advances in biofabrication. Macromol. Biosci. 19, 1800441 (2019). https://doi.org/10.1002/mabi.201800441
J. Wang, Y. Zhang, N.H. Aghda et al., Emerging 3D printing technologies for drug delivery devices: current status and future perspective. Adv. Drug Deliv. Rev. 174, 294–316 (2021). https://doi.org/10.1016/j.addr.2021.04.019
S. Zu, Z. Zhang, Q. Liu et al., 4D printing of core–shell hydrogel capsules for smart controlled drug release. Biodes. Manuf. 5, 294–304 (2022). https://doi.org/10.1007/s42242-021-00175-y
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The authors thank the financial support of the Brazilian agencies São Paulo State Research Foundation (FAPESP), Coordination for Higher Education Personnel Improvement (CAPES), Financing Studies and Projects (FINEP), and National Council of Technological and Scientific Development (CNPq).
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Piazza, R.D., dos Santos, C.C., Pinto, G.C. et al. Multifunctional Redox and Temperature-Sensitive Drug Delivery Devices. Biomedical Materials & Devices 2, 191–207 (2024). https://doi.org/10.1007/s44174-023-00101-z
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DOI: https://doi.org/10.1007/s44174-023-00101-z