Design, synthesis, characterization and evaluation of Chitosan-based hydrogel for controlled drug delivery system
- Authors: Safari, Justin Bazibuhe
- Date: 2022-04
- Subjects: Chitosan , Drug delivery systems , Drugs Controlled release , Tenofovir , Colloids , Hepatitis B Chemotherapy , Hydrogel
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10962/232182 , vital:49969
- Description: Hepatitis B infection is a deadly infectious disease caused by the hepatitis B virus and is responsible for many deaths every year worldwide. Despite medication and vaccines against hepatitis B infection, it still presents high morbidity and mortality among populations. This is partly due to factors such as a long medication period of the existing treatments, resulting in poor patient compliance and leading to treatment failure. In addition, this situation can be responsible for the observed emerging drug resistance. Hence, novel drugs and drug delivery systems are needed to tackle this matter. Many strategies have been used to develop long-acting drug delivery systems treatment for several infectious diseases. Hydrogel drug delivery systems have shown interesting results as controlled drug delivery systems for several drugs. Therefore, the present study aimed to develop chitosan grafted poly (acrylamide-co-acrylic acid) hydrogel and apply it as a pH-sensitive controlled delivery system of tenofovir disoproxil fumarate (TDF). TDF is a nucleoside reverse transcriptase inhibitor used as first-line treatment of hepatitis B chronic infection and in the treatment of other viral infections. The free-radical polymerization method was utilized to modify chitosan by grafting acrylamide and acrylic acid and using N, N’-methylene bisacrylamide as the crosslinking agent to prepare the hydrogel, followed by an optimization of parameters that could affect the swelling capacity. The prepared chitosan-g-poly(acrylamide-co-acrylic acid) hydrogel was characterized using Fourier Transmission Infra-red spectroscopy (FTIR), X-Ray Diffraction (XRD), Thermal Gravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), Energy-dispersive X-ray spectroscopy (EDS), Scanning Electron Microscopy (SEM), and was evaluated for cytotoxicity using a HeLa cell assay. TDF was used as a drug model, it was loaded by the swelling equilibrium method, following by the investigation of the release profile of TDF-loaded hydrogel at pH 1.2 and 7.4. A successful synthesis of chitosan grafted poly(acrylamide-co-acrylic acid) hydrogel was confirmed by Fourier Transmission Infra-red spectroscopy (FTIR), X-Ray Diffraction Spectroscopy (XRD), Thermal Gravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), Energy-dispersive X-ray spectroscopy (EDS) and Scanning Electron Microscopy (SEM). Optimization results showed that the ratio of monomers impacted the swelling ratio of the hydrogel and both the concentration of the crosslinking agent, and the reaction initiator also affected the swelling ratio. The synthesized hydrogels were sensitive to pH and ionic strength. Hydrogel swelling was lower in acidic solutions and higher in neutral and basic solutions and decreased with the increasing ionic strength. Furthermore, SEM results revealed that hydrogel have a rough and fibrous surface structure with numerous pores. Cytotoxicity studies demonstrated that the hydrogel was non-cytotoxic at 50 μg/ml against HeLa cells which suggested a good biocompatibility of the material. TDF was loaded and released from the hydrogels and showed an encapsulation efficiency and drug loading percentage ranging from 81-96% and 8-10%, respectively. TDF release profile was found to be low in buffer solution of pH 1.2 (in the range of 5-10%) and much higher (38-53%) at pH 7.4 within 96 hours. TDF maintained its chemical integrity after release and the hydrogels can therefore be proposed as a new controlled-release drug delivery system for hepatitis B treatment. , Thesis (MSc) -- Faculty of Science, Chemistry, 2022
- Full Text:
- Date Issued: 2022-04
- Authors: Safari, Justin Bazibuhe
- Date: 2022-04
- Subjects: Chitosan , Drug delivery systems , Drugs Controlled release , Tenofovir , Colloids , Hepatitis B Chemotherapy , Hydrogel
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10962/232182 , vital:49969
- Description: Hepatitis B infection is a deadly infectious disease caused by the hepatitis B virus and is responsible for many deaths every year worldwide. Despite medication and vaccines against hepatitis B infection, it still presents high morbidity and mortality among populations. This is partly due to factors such as a long medication period of the existing treatments, resulting in poor patient compliance and leading to treatment failure. In addition, this situation can be responsible for the observed emerging drug resistance. Hence, novel drugs and drug delivery systems are needed to tackle this matter. Many strategies have been used to develop long-acting drug delivery systems treatment for several infectious diseases. Hydrogel drug delivery systems have shown interesting results as controlled drug delivery systems for several drugs. Therefore, the present study aimed to develop chitosan grafted poly (acrylamide-co-acrylic acid) hydrogel and apply it as a pH-sensitive controlled delivery system of tenofovir disoproxil fumarate (TDF). TDF is a nucleoside reverse transcriptase inhibitor used as first-line treatment of hepatitis B chronic infection and in the treatment of other viral infections. The free-radical polymerization method was utilized to modify chitosan by grafting acrylamide and acrylic acid and using N, N’-methylene bisacrylamide as the crosslinking agent to prepare the hydrogel, followed by an optimization of parameters that could affect the swelling capacity. The prepared chitosan-g-poly(acrylamide-co-acrylic acid) hydrogel was characterized using Fourier Transmission Infra-red spectroscopy (FTIR), X-Ray Diffraction (XRD), Thermal Gravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), Energy-dispersive X-ray spectroscopy (EDS), Scanning Electron Microscopy (SEM), and was evaluated for cytotoxicity using a HeLa cell assay. TDF was used as a drug model, it was loaded by the swelling equilibrium method, following by the investigation of the release profile of TDF-loaded hydrogel at pH 1.2 and 7.4. A successful synthesis of chitosan grafted poly(acrylamide-co-acrylic acid) hydrogel was confirmed by Fourier Transmission Infra-red spectroscopy (FTIR), X-Ray Diffraction Spectroscopy (XRD), Thermal Gravimetric Analysis (TGA), Differential Scanning Calorimetry (DSC), Energy-dispersive X-ray spectroscopy (EDS) and Scanning Electron Microscopy (SEM). Optimization results showed that the ratio of monomers impacted the swelling ratio of the hydrogel and both the concentration of the crosslinking agent, and the reaction initiator also affected the swelling ratio. The synthesized hydrogels were sensitive to pH and ionic strength. Hydrogel swelling was lower in acidic solutions and higher in neutral and basic solutions and decreased with the increasing ionic strength. Furthermore, SEM results revealed that hydrogel have a rough and fibrous surface structure with numerous pores. Cytotoxicity studies demonstrated that the hydrogel was non-cytotoxic at 50 μg/ml against HeLa cells which suggested a good biocompatibility of the material. TDF was loaded and released from the hydrogels and showed an encapsulation efficiency and drug loading percentage ranging from 81-96% and 8-10%, respectively. TDF release profile was found to be low in buffer solution of pH 1.2 (in the range of 5-10%) and much higher (38-53%) at pH 7.4 within 96 hours. TDF maintained its chemical integrity after release and the hydrogels can therefore be proposed as a new controlled-release drug delivery system for hepatitis B treatment. , Thesis (MSc) -- Faculty of Science, Chemistry, 2022
- Full Text:
- Date Issued: 2022-04
Synthesis and characterization of molybdenum dichalcogenides nanoparticles via solution-processed technique for photovoltaic applications
- Authors: Shelter, Chikukwa Evernice
- Date: 2021-02
- Subjects: Nanoparticles , Colloids
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10353/20653 , vital:46417
- Description: Energy generated from non-renewable energy sources has a drawback of prompted outflow of ozone harming substances. These drawbacks of the non-renewable energy have quickened innovative work of renewable power sources, since they have an advantage of the provision of a better, preserved, decent environment that is free from natural contamination and commotion. Photovoltaic devices are prevalent in improving the green energy utilization and defeating the natural concerns yielded from the current most overwhelming energy sources. Herein, the synthesis, characterization, and application of Molybdenum chalcogenide nanoparticles (NP) as alternative sources in the absorber layer of quantum dot solar sensitized cells (QDSSCs) is discussed. The MoS2 NPs were synthesized from the aliphatic and aromatic dithiocarbamate (DTC) ligands and complexes as precursors. The successful synthesis of the DTC ligands and MoDTC complexes was confirmed through characterization with a variety of techniques including 1H and 13C-NMR, Raman Spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet-visible spectroscopy (UV-VIS), Thermogravimetric analysis (TGA) and Derivative thermogravimetric (DTG) analysis. The synthesized MoDTC complexes (precursors) were further used in the synthesis of MoS2 nanoparticles. A bottom -up colloidal approach was employed for the synthesis of the MoX2 NPs. The successful synthesis of the NP was confirmed as the results from the diffractive peaks obtained from XRD which were positive and agreed in comparison with the standard. The diffractive peaks were shown in the planes (100), (002), (100) and (105) for MoS2 nanoparticles; (002), (100), (103) and (110) for MoSe2 and (0002), (0004), (103) as well as (0006) for the MoTe2 nanoparticles. The MoSe2 nanoparticles showed the least size of the nanoparticles followed by MoTe2 and lastly MoS2. These results agreed with the results obtained using SEM analysis. For the optical properties of the nanoparticles, UV-VIS and PL were used, the shift of the peaks from the red shift (600 nm) to the blue shift 270-5 nm and 287-9 nm (UV-VIS) confirmed that the nanoparticles were quantum confined. The application of the MoX2 NPs in QDSSCs was done with MoSe2 showing the greatest PCE of 7.86 percent followed by MoTe2 6.93 percent and lastly MoS2 with a PCE of 6.05 percent and 5.47 percent. , Thesis (MSc) (Chemistry) -- University of Fort Hare, 2021
- Full Text:
- Date Issued: 2021-02
- Authors: Shelter, Chikukwa Evernice
- Date: 2021-02
- Subjects: Nanoparticles , Colloids
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10353/20653 , vital:46417
- Description: Energy generated from non-renewable energy sources has a drawback of prompted outflow of ozone harming substances. These drawbacks of the non-renewable energy have quickened innovative work of renewable power sources, since they have an advantage of the provision of a better, preserved, decent environment that is free from natural contamination and commotion. Photovoltaic devices are prevalent in improving the green energy utilization and defeating the natural concerns yielded from the current most overwhelming energy sources. Herein, the synthesis, characterization, and application of Molybdenum chalcogenide nanoparticles (NP) as alternative sources in the absorber layer of quantum dot solar sensitized cells (QDSSCs) is discussed. The MoS2 NPs were synthesized from the aliphatic and aromatic dithiocarbamate (DTC) ligands and complexes as precursors. The successful synthesis of the DTC ligands and MoDTC complexes was confirmed through characterization with a variety of techniques including 1H and 13C-NMR, Raman Spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet-visible spectroscopy (UV-VIS), Thermogravimetric analysis (TGA) and Derivative thermogravimetric (DTG) analysis. The synthesized MoDTC complexes (precursors) were further used in the synthesis of MoS2 nanoparticles. A bottom -up colloidal approach was employed for the synthesis of the MoX2 NPs. The successful synthesis of the NP was confirmed as the results from the diffractive peaks obtained from XRD which were positive and agreed in comparison with the standard. The diffractive peaks were shown in the planes (100), (002), (100) and (105) for MoS2 nanoparticles; (002), (100), (103) and (110) for MoSe2 and (0002), (0004), (103) as well as (0006) for the MoTe2 nanoparticles. The MoSe2 nanoparticles showed the least size of the nanoparticles followed by MoTe2 and lastly MoS2. These results agreed with the results obtained using SEM analysis. For the optical properties of the nanoparticles, UV-VIS and PL were used, the shift of the peaks from the red shift (600 nm) to the blue shift 270-5 nm and 287-9 nm (UV-VIS) confirmed that the nanoparticles were quantum confined. The application of the MoX2 NPs in QDSSCs was done with MoSe2 showing the greatest PCE of 7.86 percent followed by MoTe2 6.93 percent and lastly MoS2 with a PCE of 6.05 percent and 5.47 percent. , Thesis (MSc) (Chemistry) -- University of Fort Hare, 2021
- Full Text:
- Date Issued: 2021-02
Development of a low-cost bioprinting system for the fabrication of cell-laden sodium alginate hydrogels
- Authors: Honiball, John Robert
- Date: 2018
- Subjects: Regenerative medicine , Tissue engineering , Alginates , Colloids , Three-dimensional printing
- Language: English
- Type: text , Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10962/59204 , vital:27470
- Description: Bioprinting is a rapidly expanding technology with the ability to fabricate in vitro 3D tissues in a layer-by-layer manner to ultimately produce a living tissue which physiologically resembles native in vivo tissue functionality. Unfortunately, large costs associated with commercially available bioprinters severely limit the amount of people/research groups with access to the technology. Here, we investigated the potential for modifying a commercially available RepRap Prusa iteration 3 (i3) three-dimensional (3D) printer, by replacing the traditional plastic-based print-head with various open-source syringe-housed microextrusion print-head units, such that deposition of composite bioinks consisting of cells, biopolymer scaffolds and/or biomolecules may be achieved at a relatively low cost. Using adipose-derived human mesenchymal stromal stem cells (ad-HMSC) induced for adipogenic differentiation, as well as human umbilical vein endothelial cells (HUVEC), the potential for fabricating vascularised adipose tissue was investigated. The non-toxic, inexpensive algal polysaccharide, sodium alginate, was used to test the printability of the system, as well as for investigating the functionality unmodified sodium alginate has for use as a potential bioink in adipose tissue engineering. Cell viability assays, namely WST-1 and fluorescein diacetate (FDA)/propidium iodide (PI) live/dead cell staining, revealed that ad-HMSC were viable after 7 days of culture. However, viability of HUVEC encapsulated hydrogels revealed significantly lower cell viability. Live/dead cell staining revealed that the modified printing system was able to print ad-HMSC/HUVEC co-cocultures with a large degree of cell viability after 1 day of culture. However, after 7 days of culture, the majority of cells were revealed to be dead. Furthermore, due to the lack of mechanical integrity possessed by alginate in a liquid-like state, printing sodium alginate hydrogels in air consistently resulted in deformation of printed constructs. The newly developed 3D printing technique termed freeform reversible embedding of suspended hydrogels (FRESH) was therefore investigated as a means for achieving 3D spatial control of printed hydrogels using the modified system. Printing cell-free sodium alginate hydrogels within gelatin sacrificial support baths allowed for fabricating constructs in a spatially defined manner. However, overprinting and swelling of alginate hydrogels negatively affected the overall printing accuracy. The present study aimed to pave the way for further system modifications and refinements, such that the ultimate goal of low-cost bioprinting may be achieved. Further optimisation of printing parameters, hydrogel characteristics and sterilisation techniques may allow for fabricating viable, physiologically relevant tissues using the modified system developed.
- Full Text:
- Date Issued: 2018
- Authors: Honiball, John Robert
- Date: 2018
- Subjects: Regenerative medicine , Tissue engineering , Alginates , Colloids , Three-dimensional printing
- Language: English
- Type: text , Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10962/59204 , vital:27470
- Description: Bioprinting is a rapidly expanding technology with the ability to fabricate in vitro 3D tissues in a layer-by-layer manner to ultimately produce a living tissue which physiologically resembles native in vivo tissue functionality. Unfortunately, large costs associated with commercially available bioprinters severely limit the amount of people/research groups with access to the technology. Here, we investigated the potential for modifying a commercially available RepRap Prusa iteration 3 (i3) three-dimensional (3D) printer, by replacing the traditional plastic-based print-head with various open-source syringe-housed microextrusion print-head units, such that deposition of composite bioinks consisting of cells, biopolymer scaffolds and/or biomolecules may be achieved at a relatively low cost. Using adipose-derived human mesenchymal stromal stem cells (ad-HMSC) induced for adipogenic differentiation, as well as human umbilical vein endothelial cells (HUVEC), the potential for fabricating vascularised adipose tissue was investigated. The non-toxic, inexpensive algal polysaccharide, sodium alginate, was used to test the printability of the system, as well as for investigating the functionality unmodified sodium alginate has for use as a potential bioink in adipose tissue engineering. Cell viability assays, namely WST-1 and fluorescein diacetate (FDA)/propidium iodide (PI) live/dead cell staining, revealed that ad-HMSC were viable after 7 days of culture. However, viability of HUVEC encapsulated hydrogels revealed significantly lower cell viability. Live/dead cell staining revealed that the modified printing system was able to print ad-HMSC/HUVEC co-cocultures with a large degree of cell viability after 1 day of culture. However, after 7 days of culture, the majority of cells were revealed to be dead. Furthermore, due to the lack of mechanical integrity possessed by alginate in a liquid-like state, printing sodium alginate hydrogels in air consistently resulted in deformation of printed constructs. The newly developed 3D printing technique termed freeform reversible embedding of suspended hydrogels (FRESH) was therefore investigated as a means for achieving 3D spatial control of printed hydrogels using the modified system. Printing cell-free sodium alginate hydrogels within gelatin sacrificial support baths allowed for fabricating constructs in a spatially defined manner. However, overprinting and swelling of alginate hydrogels negatively affected the overall printing accuracy. The present study aimed to pave the way for further system modifications and refinements, such that the ultimate goal of low-cost bioprinting may be achieved. Further optimisation of printing parameters, hydrogel characteristics and sterilisation techniques may allow for fabricating viable, physiologically relevant tissues using the modified system developed.
- Full Text:
- Date Issued: 2018
The synthesis and properties of some polymer hydrogels
- Authors: Hird, Bryn
- Date: 1984 , 2013-04-05
- Subjects: Colloids
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:4428 , http://hdl.handle.net/10962/d1006975 , Colloids
- Description: The interactions between water molecules and polyelectrolyte species in aqueous solutions are reviewed and are used to infer interactions occuring in swollen crosslinked polyelectrolyte hydrogels. Linear poly(acrylic acid ) and derivatives neutralised to varying degrees with alkali-metal hydroxides are prepared and characterised. Samples of these compounds are crosslinked by 'Y - irradiation to form hydrogels. Hydration studies on linear polymers, crosslinked material and a commercial polyacrylate hydrogel indicate a possible hydration structure and provide some insight into the nature of water-polymer interactions within a sHollen polyacrylate gel. , KMBT_363 , Adobe Acrobat 9.53 Paper Capture Plug-in
- Full Text:
- Date Issued: 1984
- Authors: Hird, Bryn
- Date: 1984 , 2013-04-05
- Subjects: Colloids
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:4428 , http://hdl.handle.net/10962/d1006975 , Colloids
- Description: The interactions between water molecules and polyelectrolyte species in aqueous solutions are reviewed and are used to infer interactions occuring in swollen crosslinked polyelectrolyte hydrogels. Linear poly(acrylic acid ) and derivatives neutralised to varying degrees with alkali-metal hydroxides are prepared and characterised. Samples of these compounds are crosslinked by 'Y - irradiation to form hydrogels. Hydration studies on linear polymers, crosslinked material and a commercial polyacrylate hydrogel indicate a possible hydration structure and provide some insight into the nature of water-polymer interactions within a sHollen polyacrylate gel. , KMBT_363 , Adobe Acrobat 9.53 Paper Capture Plug-in
- Full Text:
- Date Issued: 1984
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