Review Article
Thermosensitive Chitosan-β-Glycerophosphate Hydrogels as Targeted Drug Delivery Systems: An Overview on Preparation and Their Applications
Table 1
Type of thermo-responsive hydrogels.
| | Polymers combined with | Gelling temperature °C | In the market | Disadvantages | Advantages | Application | Reference |
| 1. Cellulose derivative | | | | | | | | 1.1 methylcellulose | N-isopropyl acrylamide (NiPAAM) | 60–80 | | | | Create a bioactive scaffold | [14] | 1.2 chitosan | PEG [15] N-isopropyl acrylamide (NiPAAM) [16] Glycerophosphate [17] | 37 | BST-Gel ® [18] | The initial release of the drug is high. It always retains some of the drugs. It has a low rate of destruction | Forms a reversible gel that gels when placed in the body. It can release the drug for a long time. Biodegradable and good biocompatibility | Cell delivery Drug delivery Implant Similar structure to extracellular matrix | [17] | 1.3 Dextran | N-isopropyl acrylamide (NiPAAM) | 32–37 | | At a temperature of 37 degrees, its degradation rate decreases. Drug release depends on various factors such as pH and electrolyte | It can create a sustained release formulation | Drug delivery | [19] |
| 2. Proteins | | | | | | | | 2.1 Gelatine | Poly(ethylene glycol)-Poly (D, L-lactic) (mPEG-DLLA) [20] | Below 25 | | Improper gelling and adhesion properties The initial release of the drug is high | Slow-release profile | Drug release kinetic with gentamycin sulfate | [21] |
| Other polymers | | | | | | | | 3. N-isopropylacrylamide | | 32 | | Nonbiodegradable The gelling temperature depends on the pH and electrolytes of the environment. Swelling was lower Initial burst release | Preparation of implants Long-term drug release | Drug delivery Cell encapsulation Cell culture Biomedical engineering application | [22] | 4. PEO/PPO Poloxamer ® | Poly (ether-carbonate) | 37 | LeGoo ® [23] | Lower stiffness than other hydrogels After one week degraded | Biocompatible High viscosity | Drug and gene delivery Tissue adhesive Burn wound covering | [24, 25] |
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