Abstract:Cancer is the leading cause of death after cardiovascular disease. Despite significant advances in cancer research over the past few decades, it is almost impossible to cure end-stage cancer patients and bring them to remission. Adverse effects of chemotherapy are mainly caused by the accumulation of chemotherapeutic agents in normal tissues, and drug resistance hinders the potential therapeutic effects and curing of this disease. New drug formulations need to be developed to overcome these problems and increa… Show more
“…118 The stability of sensitive therapeutics such as small proteins, monoclonal antibodies, and nucleic acids within the scaffolds should also be studied. 119 3.2. Hydrogels.…”
Section: Biomaterial-based Sustained-release Platforms Developed For ...mentioning
confidence: 99%
“…Furthermore, natural and synthetic hydrogels have their own characteristic properties; natural hydrogels can inherit the original bioactivity that can potentiate the drug actions, and synthetic hydrogels can be better tailored to desired mechanical properties, biodegradability, and toxicity profiles by the synthetic modification of polymers. 119 Microneedle patches are ideal for precisely controlled drug delivery in a small area of skin layers, whereas inorganic scaffolds and hydrogels can only be administered in bulk quantity to large areas of deeper tissues. In addition, microneedles can avoid the injury and pain caused by needle-stick injections.…”
Section: Perspectivesmentioning
confidence: 99%
“…Overall, the fabrication of inorganic scaffolds should thoroughly investigate and optimize the parameters of inorganic materials potentially implicated in the in vivo toxicity and drug release profiles . The stability of sensitive therapeutics such as small proteins, monoclonal antibodies, and nucleic acids within the scaffolds should also be studied …”
Section: Biomaterial-based Sustained-release Platforms
Developed For ...mentioning
confidence: 99%
“…Their soft nature and high water content are also well suited for the manufacturing of injectable drug formulations with enhanced biodegradability and biocompatibility compared with those of inorganic scaffolds. Furthermore, natural and synthetic hydrogels have their own characteristic properties; natural hydrogels can inherit the original bioactivity that can potentiate the drug actions, and synthetic hydrogels can be better tailored to desired mechanical properties, biodegradability, and toxicity profiles by the synthetic modification of polymers . Microneedle patches are ideal for precisely controlled drug delivery in a small area of skin layers, whereas inorganic scaffolds and hydrogels can only be administered in bulk quantity to large areas of deeper tissues.…”
Cancer immunotherapy has revolutionized clinical cancer treatments by taking advantage of the immune system to selectively and effectively target and kill cancer cells. However, clinical cancer immunotherapy treatments often have limited efficacy and/or present severe adverse effects associated primarily with their systemic administration. Localized immunotherapy has emerged to overcome these limitations by directly targeting accessible tumors via local administration, reducing potential systemic drug distribution that hampers drug efficacy and safety. Sustained-release formulations can prolong drug activity at target sites, which maximizes the benefits of localized immunotherapy to increase the therapeutic window using smaller dosages than those used for systemic injection, avoiding complications of frequent dosing. The performance of sustained-release formulations for localized cancer immunotherapy has been validated preclinically using various implantable and injectable scaffold platforms. This review introduces the sustained-release formulations developed for localized cancer immunotherapy and highlights their biomaterial-based platforms for representative classes, including inorganic scaffolds, natural hydrogels, synthetic hydrogels, and microneedle patches. The design rationale and other considerations are summarized for further development of biomaterials for the construction of optimal sustained-release formulations.
“…118 The stability of sensitive therapeutics such as small proteins, monoclonal antibodies, and nucleic acids within the scaffolds should also be studied. 119 3.2. Hydrogels.…”
Section: Biomaterial-based Sustained-release Platforms Developed For ...mentioning
confidence: 99%
“…Furthermore, natural and synthetic hydrogels have their own characteristic properties; natural hydrogels can inherit the original bioactivity that can potentiate the drug actions, and synthetic hydrogels can be better tailored to desired mechanical properties, biodegradability, and toxicity profiles by the synthetic modification of polymers. 119 Microneedle patches are ideal for precisely controlled drug delivery in a small area of skin layers, whereas inorganic scaffolds and hydrogels can only be administered in bulk quantity to large areas of deeper tissues. In addition, microneedles can avoid the injury and pain caused by needle-stick injections.…”
Section: Perspectivesmentioning
confidence: 99%
“…Overall, the fabrication of inorganic scaffolds should thoroughly investigate and optimize the parameters of inorganic materials potentially implicated in the in vivo toxicity and drug release profiles . The stability of sensitive therapeutics such as small proteins, monoclonal antibodies, and nucleic acids within the scaffolds should also be studied …”
Section: Biomaterial-based Sustained-release Platforms
Developed For ...mentioning
confidence: 99%
“…Their soft nature and high water content are also well suited for the manufacturing of injectable drug formulations with enhanced biodegradability and biocompatibility compared with those of inorganic scaffolds. Furthermore, natural and synthetic hydrogels have their own characteristic properties; natural hydrogels can inherit the original bioactivity that can potentiate the drug actions, and synthetic hydrogels can be better tailored to desired mechanical properties, biodegradability, and toxicity profiles by the synthetic modification of polymers . Microneedle patches are ideal for precisely controlled drug delivery in a small area of skin layers, whereas inorganic scaffolds and hydrogels can only be administered in bulk quantity to large areas of deeper tissues.…”
Cancer immunotherapy has revolutionized clinical cancer treatments by taking advantage of the immune system to selectively and effectively target and kill cancer cells. However, clinical cancer immunotherapy treatments often have limited efficacy and/or present severe adverse effects associated primarily with their systemic administration. Localized immunotherapy has emerged to overcome these limitations by directly targeting accessible tumors via local administration, reducing potential systemic drug distribution that hampers drug efficacy and safety. Sustained-release formulations can prolong drug activity at target sites, which maximizes the benefits of localized immunotherapy to increase the therapeutic window using smaller dosages than those used for systemic injection, avoiding complications of frequent dosing. The performance of sustained-release formulations for localized cancer immunotherapy has been validated preclinically using various implantable and injectable scaffold platforms. This review introduces the sustained-release formulations developed for localized cancer immunotherapy and highlights their biomaterial-based platforms for representative classes, including inorganic scaffolds, natural hydrogels, synthetic hydrogels, and microneedle patches. The design rationale and other considerations are summarized for further development of biomaterials for the construction of optimal sustained-release formulations.
“…Until now, AM was associated with various biological uses, which inspired novel printing techniques to emerge and had been constantly improved upon to suit different unmet clinical needs [19]. This cost-efficient technique exploits biocompatible materials and is used to develop novel model implants to provide a greater understanding of human anatomy and diseases, and can be used for organ transplants, surgical planning, and the manufacturing of advanced drug delivery systems [20,21]. In addition, nowadays, 3D-printed medical devices and implants can be designed and customized for each patient to provide a more tailored treatment approach.…”
Three-dimensional printing technology has emerged as a promising tool for meticulously fabricated scaffolds with high precision and accuracy, resulting in intricately detailed biomimetic 3D structures. Producing magnetic scaffolds with the aid of additive processes, known as 3D printing, reveals multitude and state-of-the-art areas of application such as tissue engineering, bone repair and regeneration, drug delivery and magnetic hyperthermia. A crucial first step is the development of innovative polymeric composite magnetic materials. The current work presents a fabrication protocol of 3D printed polymer-bonded magnets using the Fused Deposition Modeling 3D printing method. Polymer-bonded magnets are defined as composites with permanent-magnet powder embedded in a polymer binder matrix. By using a low-cost mixing extruder, four (4) different filament types of 1.75 mm were fabricated using commercial magnetite magnetic nanoparticles mixed with a pure polylactic acid powder (PLA) and a ferromagnetic PLA (Iron particles included) filaments. The powder mixture of the basic filaments was compounded mixed with the nanoparticles, and extruded to fabricate the 3D printing filament, which is subsequently characterized structurally and magnetically before the printing process. Magnetic polymer scaffolds are finally printed using composite filaments of different concentration in magnetite. Our results demonstrate that the heating efficiency (expressed in W/g) of the 3D printed magnetic polymer scaffolds (ranging from 2 to 5.5 W/g at magnetic field intensity of 30 mT and field frequency of 365 kHz) can be tuned by choosing either a magnetic or a non-magnetic filament mixed with an amount of magnetite nanoparticles in different concentrations of 10 or 20 wt %. Our work opens up new perspectives for future research, such as the fabrication of complex structures with suitable ferromagnetic custom-made filaments adjusting the mixing of different filaments for the construction of scaffolds aimed at improving the accuracy of magnetic hyperthermia treatment.
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