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Sarmad, S., Nikjoo, D. & Mikkola, J.-P. (2025). Innovative CO2 capture technologies: Exploring the potential of porous liquids containing deep eutectic solvents and hypercrosslinked polymers. Separation and Purification Technology, 352, Article ID 128189.
Öppna denna publikation i ny flik eller fönster >>Innovative CO2 capture technologies: Exploring the potential of porous liquids containing deep eutectic solvents and hypercrosslinked polymers
2025 (Engelska)Ingår i: Separation and Purification Technology, ISSN 1383-5866, E-ISSN 1873-3794, Vol. 352, artikel-id 128189Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The current study presented a porous liquid (PL) prepared from propylene glycol-based deep eutectic solvent (DES) and hyper-crosslinked polymers (HCP) that are liquids over wide temperature ranges, including ambient temperature. It was shown that the solvent molecules are too large to penetrate the pores of HCP, so the PL is maintained as a suspension with permanent free volume for several months and can absorb large amounts of gases. This study marks the pioneering use of DESs as the liquid medium, replacing ionic liquids due to their closely matched properties. The structural features of both DES and HCP are retained; the increase in CO2 absorption capacity compared to pure DES is due to the presence of a porous solid and is proportional to the amount of solid. The absorbed CO2 amount rises from 1.0105 mmol·g−1 in pure DES to 1.3232, 1.6027, and 1.2168 mmol·g−1 in PL-1, PL-2, and PL-3, respectively. Thermodynamic analysis revealed that the enthalpy of gas absorption allows straightforward regeneration of the PLs in the studied cases. The investigated PLs show great potential as gas absorbents, with the incorporation of just 0.5 wt% of porous polymer material leading to an impressive increase in solvent absorption capacity, up to 59 %.

Ort, förlag, år, upplaga, sidor
Elsevier B.V., 2025
Nyckelord
CO2 capture, Deep eutectic solvent, Hypercrosslinked polymers, Porous liquids, Propylene glycol
Nationell ämneskategori
Energiteknik
Forskningsämne
Materialteknik
Identifikatorer
urn:nbn:se:ltu:diva-107424 (URN)10.1016/j.seppur.2024.128189 (DOI)2-s2.0-85194943480 (Scopus ID)
Anmärkning

Godkänd;2024;Nivå 0;2024-06-14 (joosat);

Full text license: CC BY

Tillgänglig från: 2024-06-14 Skapad: 2024-06-14 Senast uppdaterad: 2024-06-14Bibliografiskt granskad
Velarde, L., Nikjoo, D., Escalera, E. & Akhtar, F. (2024). Bolivian natural zeolite as a low-cost adsorbent for the adsorption of cadmium: Isotherms and kinetics. Heliyon, 10(1), Article ID e24006.
Öppna denna publikation i ny flik eller fönster >>Bolivian natural zeolite as a low-cost adsorbent for the adsorption of cadmium: Isotherms and kinetics
2024 (Engelska)Ingår i: Heliyon, E-ISSN 2405-8440, Vol. 10, nr 1, artikel-id e24006Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Population growth in recent years has led to increased wastewater production and pollution of water resources. This situation also heavily affects Bolivia, so wastewater treatment methods and materials suitable for Bolivian society should be explored. This study investigated the natural Bolivian Zeolite (BZ) and its NaCl-modified structure (NaBZ) as adsorbents for cadmium removal from water. The natural BZ and the modified form NaBZ were investigated by different physicochemical characterization techniques. Furthermore, XPS and FT-IR techniques were used to investigate the adsorption mechanisms. The cadmium adsorption on BZ and NaBZ was analyzed using various mathematical models, and the Langmuir model provided a better description of the experimental adsorption data with cadmium adsorption capacities of 20.2 and 25.6 mg/g for BZ and NaBZ, respectively. The adsorption followed the pseudo-second order kinetics. The effect of different parameters, such as initial cadmium concentration and pH on the adsorption was studied. In addition, the results of the regeneration test indicated that both BZ and NaBZ can be regenerated by using hydrochloric acid (HCl). Finally, the adsorption experiment of BZ and NaBZ on a real water sample (brine from Salar de Uyuni salt flat) containing a mixture of different heavy metals was carried out. The results obtained in this study demonstrate the effectiveness of natural BZ and modified NaBZ in the removal of heavy metals from wastewater.

Ort, förlag, år, upplaga, sidor
Elsevier, 2024
Nyckelord
Adsorption, Cadmium, Clinoptilolite, Heavy metals, Natural zeolites
Nationell ämneskategori
Organisk kemi
Forskningsämne
Materialteknik
Identifikatorer
urn:nbn:se:ltu:diva-103749 (URN)10.1016/j.heliyon.2024.e24006 (DOI)001156685700001 ()38234893 (PubMedID)2-s2.0-85181824101 (Scopus ID)
Forskningsfinansiär
Sida - Styrelsen för internationellt utvecklingssamarbete, 13486
Anmärkning

Validerad;2024;Nivå 2;2024-02-01 (signyg);

Full text license: CC BY

Tillgänglig från: 2024-01-16 Skapad: 2024-01-16 Senast uppdaterad: 2024-04-19Bibliografiskt granskad
Khasevani, S. G., Nikjoo, D., Chaxel, C., Umeki, K., Sarmad, S., Mikkola, J.-P. & Concina, I. (2023). Empowering Adsorption and Photocatalytic Degradation of Ciprofloxacin on BiOI Composites: A Material-by-Design Investigation. ACS Omega, 8(46), 44044-44056
Öppna denna publikation i ny flik eller fönster >>Empowering Adsorption and Photocatalytic Degradation of Ciprofloxacin on BiOI Composites: A Material-by-Design Investigation
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2023 (Engelska)Ingår i: ACS Omega, E-ISSN 2470-1343, Vol. 8, nr 46, s. 44044-44056Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Binary and ternary composites of BiOI with NH2-MIL-101(Fe) and a functionalized biochar were synthesized through an in situ approach, aimed at spurring the activity of the semiconductor as a photocatalyst for the removal of ciprofloxacin (CIP) from water. Experimental outcomes showed a drastic enhancement of the adsorption and the equilibrium (which increased from 39.31 mg g–1 of bare BiOI to 76.39 mg g–1 of the best ternary composite in 2 h time), while the kinetics of the process was not significantly changed. The photocatalytic performance was also significantly enhanced, and the complete removal of 10 ppm of CIP in 3 h reaction time was recorded under simulated solar light irradiation for the best catalyst of the investigated batch. Catalytic reactions supported by different materials obeyed different reaction orders, indicating the existence of different mechanisms. The use of scavengers for superoxide anion radicals, holes, and hydroxyl radicals showed that although all these species are involved in CIP photodegradation, the latter play the most crucial role, as also confirmed by carrying out the reaction at increasing pH conditions. A clear correlation between the reduction of BiOI crystallite sizes in the composites, as compared to the bare material, and the material performance as both adsorbers and photocatalyst was identified. 

Ort, förlag, år, upplaga, sidor
American Chemical Society (ACS), 2023
Nationell ämneskategori
Fysikalisk kemi Materialkemi
Forskningsämne
Energiteknik; Experimentell fysik; Avfallsteknik
Identifikatorer
urn:nbn:se:ltu:diva-103204 (URN)10.1021/acsomega.3c06243 (DOI)001108005100001 ()2-s2.0-85178352921 (Scopus ID)
Forskningsfinansiär
Kempestiftelserna, SMK-1974Knut och Alice Wallenbergs StiftelseBio4Energy
Anmärkning

Validerad;2023;Nivå 2;2023-12-11 (joosat);

License full text: CC BY

Tillgänglig från: 2023-12-11 Skapad: 2023-12-11 Senast uppdaterad: 2024-03-07Bibliografiskt granskad
Nikjoo, D., van der Zwaan, I., Rudén, J. & Frenning, G. (2023). Engineered microparticles of hyaluronic acid hydrogel for controlled pulmonary release of salbutamol sulphate. International Journal of Pharmaceutics, 643, Article ID 123225.
Öppna denna publikation i ny flik eller fönster >>Engineered microparticles of hyaluronic acid hydrogel for controlled pulmonary release of salbutamol sulphate
2023 (Engelska)Ingår i: International Journal of Pharmaceutics, ISSN 0378-5173, E-ISSN 1873-3476, Vol. 643, artikel-id 123225Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Most pulmonary drugs are immediate-release formulations with short duration of action. Controlled release systems provide the ability to deliver drugs at a controlled rate, which helps maintain drug concentrations within the therapeutic window for a longer period of time. This study aimed to produce microparticles (MPs) of hyaluronic acid hydrogel (HAGA) loaded with salbutamol sulphate (SS) for controlled release in the lung. The drug-loaded MPs were prepared via spray drying and underwent extensive characterization, which revealed that SS was successfully encapsulated in the HAGA matrix. The prepared MPs (denoted as HASS) ranged in size from 1.6 ± 0.4 μm to 1.7 ± 0.5 μm with a fine particle fraction (FPF) of 48–56% and showed improvement in aerodynamic properties compared to unloaded HAGA hydrogel MPs. In vitro drug release studies performed in a Transwell system confirmed the potential of the particles to release the drug in a sustained manner. The drug release was delayed for all formulations, with a t63 between 5 and 30 min, compared to <1min for pure SS. This study advances our understanding of the formulation of a highly soluble drug to achieve controlled release in the lung.

Ort, förlag, år, upplaga, sidor
Elsevier, 2023
Nyckelord
Hyaluronic acid, Salbutamol sulphate, Hydrogel, Controlled release, Pulmonary
Nationell ämneskategori
Farmaceutiska vetenskaper
Forskningsämne
Materialteknik
Identifikatorer
urn:nbn:se:ltu:diva-99261 (URN)10.1016/j.ijpharm.2023.123225 (DOI)001049344600001 ()37451326 (PubMedID)2-s2.0-85166569074 (Scopus ID)
Forskningsfinansiär
Vinnova, 2017-02690
Anmärkning

Godkänd;2023;Nivå 0;2023-08-07 (hanlid)

Tillgänglig från: 2023-08-07 Skapad: 2023-08-07 Senast uppdaterad: 2023-10-11Bibliografiskt granskad
Khokarale, S. G., Jablonski, P., Nikjoo, D., Dinh, V. M., Sundman, O., Irgum, K. & Mikkola, J.-P. (2022). Poly (Vinylidene Difluoride) Polymer in 1-Ethyl-3-methylimidazolium Acetate and Acetic Acid Containing Solvents: Tunable and Recoverable Solvent Media to Induce Crystalline Phase Transition and Porosity. Sustainable Chemistry, 3(4), 455-474
Öppna denna publikation i ny flik eller fönster >>Poly (Vinylidene Difluoride) Polymer in 1-Ethyl-3-methylimidazolium Acetate and Acetic Acid Containing Solvents: Tunable and Recoverable Solvent Media to Induce Crystalline Phase Transition and Porosity
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2022 (Engelska)Ingår i: Sustainable Chemistry, E-ISSN 2673-4079, Vol. 3, nr 4, s. 455-474Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

In this report, 1-ethyl-3-methylimidazolium acetate, [EMIM][AcO] ionic liquid (IL) and acetic acid (AA) comprised solvents were used for the thermal treatment of poly (vinylidene difluoride), PVDF. Here, besides the various combinations of IL and AA in solvents, the pure IL and AA were also applied as a solvent upon thermal treatments. The samples obtained after the treatment were analysed for structural and crystalline phase changes, porosity, and molecular weight distribution with various analytical techniques. The Kamlet-Taft parameters measurement of the IL and AA containing solvents with different solvatochromic dyes was also performed to examine their solvent properties and correlate with the properties of the treated PVDF materials. The treatment of PVDF with pure IL results in the formation of highly carbonaceous material due to extensive dehydroflurination (DHF) as well as possibly successive cross-linking in the polymer chains. Upon IL and AA combined solvent treatment, the neat PVDF which composed of both α- and β crystalline phases was transformed to porous and β-phase rich material whereas in case of pure AA the non-porous and pure α-phase polymeric entity was obtained. A combined mixture of IL and AA resulted in a limited the DHF process and subsequent cross-linking in the polymer chains of PVDF allowed the formation of a porous material. It was observed that the porosity of the thermally treated materials was steadily decreasing with increase in the amount of AA in solvents composition and solvent with an AA:IL mole ratio of 2:1 resulted in a PVDF material with the highest porosity amongst the applied solvents. A recovery method for the IL and AA combined solvent after the thermal treatment of PVDF was also established. Hence, with varying the type of solvents in terms of composition, the highly carbonaceous materials as well as materials with different porosities as well as crystalline phases can be obtained. Most importantly here, we introduced new IL and AA containing recoverable solvents for the synthesis of porous PVDF material with the electroactive β-phase.

Ort, förlag, år, upplaga, sidor
MDPI, 2022
Nyckelord
poly (vinylidene difluoride), ionic liquid, acetic acid, crystalline phase transition, porosity, recoverable solvents
Nationell ämneskategori
Polymerteknologi Materialkemi
Forskningsämne
Materialteknik
Identifikatorer
urn:nbn:se:ltu:diva-95037 (URN)10.3390/suschem3040028 (DOI)
Anmärkning

Godkänd;2022;Nivå 0;2022-12-29 (johcin)

Tillgänglig från: 2022-12-28 Skapad: 2022-12-28 Senast uppdaterad: 2023-02-17Bibliografiskt granskad
Mukesh, C., Sarmad, S., Samikannu, A., Nikjoo, D., Siljebo, W. & Mikkola, J.-P. (2022). Pore size-excluded low viscous porous liquids for CO2 sorption at room temperature and thermodynamic modeling study. Journal of Molecular Liquids, 356, Article ID 119046.
Öppna denna publikation i ny flik eller fönster >>Pore size-excluded low viscous porous liquids for CO2 sorption at room temperature and thermodynamic modeling study
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2022 (Engelska)Ingår i: Journal of Molecular Liquids, ISSN 0167-7322, E-ISSN 1873-3166, Vol. 356, artikel-id 119046Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Herein, we report porous ionic liquids (type-III) designed to utilize microporous ZIF-8 moieties with functional ionic liquids such as 8-(2-methoxyethyl)-1,8-Diazabicyclo[5.4.0]undec-7-en-8-ium, Bis(trifluoromethane)sulfonamide ([MEDBU][TFSI] and Trioctylammonium 4-para-tert-butylbenzoiate [TOAH][PTBBA]). The prepared materials were thoroughly characterized by means of XRD, FT-IR, SEM, TEM, BET, TGA, DSC and viscometry techniques. The idea of combining the intrinsic properties of ionic liquids with microporous architecture to prepare porous ionic liquids yields promising fluidic materials that have received attention in industrial applications such as gas sorption and separation etc. The prepared porous ionic liquids possess unique physico-chemical properties such as low viscosity, high thermal stability, low vapor pressure, reusability and their fluidic nature renders the materials suitable for CO2 capture. Herein introduced porous ionic liquids (ILs) showed enhanced CO2 uptake (0.92 mmol/g in [TOAH][PTBBA]-Z100 and 1.16 mmol/g in [MEDBU][TFSI]-Z200), or in other words, 15–47% higher sorption capacity compared to neat ionic liquids. This concept overcomes the drawbacks of highly viscous ILs and their limited CO2 sorption capacity. Thermodynamic modeling further demonstrated that the enthalpy of sorption is only −9.99 kJ mol−1, indicating that significantly less energy is required for regeneration. This is promising for the potential use of these fluidic materials in continuous separation processes on an industrial scale, as a better alternative to the existing hazardous amine scrubbing.

Ort, förlag, år, upplaga, sidor
Elsevier, 2022
Nyckelord
Porous ionic liquids, Reversible CO2 capture, ZIF-8, Ionic liquids
Nationell ämneskategori
Energiteknik
Forskningsämne
Materialteknik
Identifikatorer
urn:nbn:se:ltu:diva-90063 (URN)10.1016/j.molliq.2022.119046 (DOI)000799182800017 ()2-s2.0-85128835880 (Scopus ID)
Forskningsfinansiär
Bio4EnergyKempestiftelsernaKnut och Alice Wallenbergs Stiftelse
Anmärkning

Validerad;2022;Nivå 2;2022-04-13 (joosat);

Tillgänglig från: 2022-04-04 Skapad: 2022-04-04 Senast uppdaterad: 2022-08-02Bibliografiskt granskad
Jablonski, P., Nikjoo, D., Warna, J., Irgum, K., Mikkola, J.-P. & Khokarale, S. G. (2022). Sustainable, highly selective, and metal-free thermal depolymerization of poly-(3-hydroxybutyrate) to crotonic acid in recoverable ionic liquids. Green Chemistry, 24(10), 4130-4139
Öppna denna publikation i ny flik eller fönster >>Sustainable, highly selective, and metal-free thermal depolymerization of poly-(3-hydroxybutyrate) to crotonic acid in recoverable ionic liquids
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2022 (Engelska)Ingår i: Green Chemistry, ISSN 1463-9262, E-ISSN 1463-9270, Vol. 24, nr 10, s. 4130-4139Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Valorization of renewable and biodegradable biopolymers to value added chemicals and green fuels is currently considered as an important research topic aiming at reducing the dependency on fossil derived feedstocks as well as their negative consequences on the environment. In this report, we are introducing an ionic liquid (IL) mediated, sustainable, and green synthesis of crotonic acid (CA) from poly-(3-hydroxybutyrate, PHB), a biopolymer derived from microbial fermentation. In this actual case, imidazolium cation comprising ILs have been used in the synthesis, where the influence of various reaction parameters such as reaction temperature and types of ILs as well as the amount of polymer, water, and IL in the reaction mixture were examined. The conversion of PHB to CA in IL took place by a base catalyzed depolymerization with formation of crotonyl terminated polymeric entities as intermediates, a mechanism that was confirmed by NMR analysis of the reaction mixtures sampled when the reactions were carried out at various temperatures. The rate of CA formation via the IL mediated base catalyzed depolymerization increased with increasing temperature in the tested interval, and 97% yield of CA was obtained after 90 min at 140 degrees C. The [EMIM][AcO] IL applied as solvent and catalyst is capable of completely depolymerizing PHB to CA in 5 h at 120 degrees C up to a polymer loading of 40 wt%. At higher loadings the depolymerization became incomplete, which is attributed to a deactivation of the IL due to hydrogen bonding interactions with the in situ formed CA, confirmed by NMR and DSC techniques. Since the depolymerization is base catalyzed, the only tested ILs that were able to form CA were based on acetate anions, whereas the less basic or neutral [EMIM][Cl] IL was found to be inactive. Finally, more than 90% of CA as well as [EMIM][AcO] IL were recovered in high purity by solvent extraction with brine (saturated aqueous NaCl) and 2-methyl tetrahydrofuran (2-Me-THF). Most importantly, here we introduce a sustainable, metal free, and single solvent based reaction approach for selective depolymerization of PHB to industrially valuable CA in basic and recoverable ILs.

Ort, förlag, år, upplaga, sidor
Royal Society of Chemistry, 2022
Nationell ämneskategori
Analytisk kemi Polymerkemi Energisystem
Forskningsämne
Materialteknik
Identifikatorer
urn:nbn:se:ltu:diva-90716 (URN)10.1039/d2gc00621a (DOI)000792782700001 ()2-s2.0-85131448220 (Scopus ID)
Forskningsfinansiär
Vetenskapsrådet, 2016-02011 MISTRAKnut och Alice Wallenbergs Stiftelse
Anmärkning

Validerad;2022;Nivå 2;2022-05-24 (hanlid)

Tillgänglig från: 2022-05-24 Skapad: 2022-05-24 Senast uppdaterad: 2022-07-11Bibliografiskt granskad
Khasevani, S. G., Nikjoo, D., Ojwang, D. O., Nodari, L., Sarmad, S., Mikkola, J.-P., . . . Concina, I. (2022). The beauty of being complex: Prussian blue analogues as selective catalysts and photocatalysts in the degradation of ciprofloxacin. Journal of Catalysis, 410, 307-319
Öppna denna publikation i ny flik eller fönster >>The beauty of being complex: Prussian blue analogues as selective catalysts and photocatalysts in the degradation of ciprofloxacin
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2022 (Engelska)Ingår i: Journal of Catalysis, ISSN 0021-9517, E-ISSN 1090-2694, Vol. 410, s. 307-319Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

We investigate the performance of four Prussian blue analogues (PBAs) as catalysts for the selective degradation of ciprofloxacin in water, under both dark and illumination conditions. We show that no light is actually needed to induce a selective degradation of the molecular target, while light irradiation spurs the process, without, however, resulting in the commonly reported photolysis-supported breaking down. We present a systematic characterization of the PBAs aiming at interpreting the catalytic outcomes in the light of a classic coordination chemistry analysis, empowered by the most recent findings in literature. We show that varying the transition metal binding the N atom of the cyanide bridge is key to promote photoinduced charge generation and transfer, which effectively disrupts the molecular target. The analysis of the materials before and after the irradiation with solar simulated light results in a change of the lattice parameters, indicating the possibility of a light-induced spin cross-over.

Ort, förlag, år, upplaga, sidor
Elsevier, 2022
Nyckelord
Prussian blue analogues, Ciprofloxacin degradation, Photocatalysis, Auto-catalytic reactions, Mössbauer spectroscopy
Nationell ämneskategori
Materialkemi Fysikalisk kemi
Forskningsämne
Materialteknik; Experimentell fysik
Identifikatorer
urn:nbn:se:ltu:diva-90488 (URN)10.1016/j.jcat.2022.04.029 (DOI)000799277700002 ()2-s2.0-85129740965 (Scopus ID)
Forskningsfinansiär
Kempestiftelserna, (SMK-1947)ÅForsk (Ångpanneföreningens Forskningsstiftelse), (18-459)Energimyndigheten, (45517-1)
Anmärkning

Validerad;2022;Nivå 2;2022-05-11 (sofila)

Tillgänglig från: 2022-05-02 Skapad: 2022-05-02 Senast uppdaterad: 2022-06-20Bibliografiskt granskad
Nikjoo, D., van der Zwaan, I., Brülls, M., Tehler, U. & Frenning, G. (2021). Hyaluronic Acid Hydrogels for Controlled Pulmonary Drug Delivery—A Particle Engineering Approach. Pharmaceutics, 13(11), Article ID 1878.
Öppna denna publikation i ny flik eller fönster >>Hyaluronic Acid Hydrogels for Controlled Pulmonary Drug Delivery—A Particle Engineering Approach
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2021 (Engelska)Ingår i: Pharmaceutics, ISSN 1999-4923, E-ISSN 1999-4923, Vol. 13, nr 11, artikel-id 1878Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Hydrogels warrant attention as a potential material for use in sustained pulmonary drug delivery due to their swelling and mucoadhesive features. Herein, hyaluronic acid (HA) is considered a promising material due to its therapeutic potential, the effect on lung inflammation, and possible utility as an excipient or drug carrier. In this study, the feasibility of using HA hydrogels (without a model drug) to engineer inhalation powders for controlled pulmonary drug delivery was assessed. A combination of chemical crosslinking and spray-drying was proposed as a novel methodology for the preparation of inhalation powders. Different crosslinkers (urea; UR and glutaraldehyde; GA) were exploited in the hydrogel formulation and the obtained powders were subjected to extensive characterization. Compositional analysis of the powders indicated a crosslinked structure of the hydrogels with sufficient thermal stability to withstand spray drying. The obtained microparticles presented a spherical shape with mean diameter particle sizes from 2.3 ± 1.1 to 3.2 ± 2.9 μm. Microparticles formed from HA crosslinked with GA exhibited a reasonable aerosolization performance (fine particle fraction estimated as 28 ± 2%), whereas lower values were obtained for the UR-based formulation. Likewise, swelling and stability in water were larger for GA than for UR, for which the results were very similar to those obtained for native (not crosslinked) HA. In conclusion, microparticles could successfully be produced from crosslinked HA, and the ones crosslinked by GA exhibited superior performance in terms of aerosolization and swelling.

Ort, förlag, år, upplaga, sidor
MDPI, 2021
Nyckelord
hyaluronic acid, salbutamol sulphate, spray-drying, urea, glutaraldehyde, drug delivery
Nationell ämneskategori
Polymerkemi
Forskningsämne
Materialteknik
Identifikatorer
urn:nbn:se:ltu:diva-88012 (URN)10.3390/pharmaceutics13111878 (DOI)000726994300001 ()34834293 (PubMedID)2-s2.0-85118747181 (Scopus ID)
Forskningsfinansiär
Vinnova, 2017-02690; 2019-00048Vinnova
Anmärkning

Validerad;2021;Nivå 2;2021-11-25 (beamah)

Tillgänglig från: 2021-11-25 Skapad: 2021-11-25 Senast uppdaterad: 2021-12-13Bibliografiskt granskad
Elbadawi, M., Nikjoo, D., Gustafsson, T., Gaisford, S. & Basit, A. (2021). Pressure-assisted microsyringe 3D printing of oral films based on pullulan and hydroxypropyl methylcellulose. International Journal of Pharmaceutics, 595, Article ID 120197.
Öppna denna publikation i ny flik eller fönster >>Pressure-assisted microsyringe 3D printing of oral films based on pullulan and hydroxypropyl methylcellulose
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2021 (Engelska)Ingår i: International Journal of Pharmaceutics, ISSN 0378-5173, E-ISSN 1873-3476, Vol. 595, artikel-id 120197Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Oral films (OFs) continue to attract attention as drug delivery systems, particularly for pedatric and geriatric needs. However, immiscibility between different polymers limits the full potential of OFs from being explored. One example is pullulan (PUL), a novel biopolymer which often has to be blended with other polymers to reduce cost and alter its mechanical properties. In this study, the state-of-the-art in fabrication techniques, three-dimensional (3D) printing was used to produce hybrid film structures of PUL and hydroxypropyl methylcellulose (HPMC), which were loaded with caffeine as a model drug. 3D printing was used to control the spatial deposition of films. HPMC was found to increase the mean mechanical properties of PUL films, where the tensile strength, elastic modulus and elongation break increased from 8.9 to 14.5 MPa, 1.17 to 1.56 GPa and from 1.48% to 1.77%, respectively. In addition, the spatial orientation of the hybrid films was also explored to determine which orientation could maximize the mechanical properties of the hybrid films. The results revealed that 3D printing could modify the mechanical properties of PUL whilst circumventing the issues associated with immiscibility.

Ort, förlag, år, upplaga, sidor
Elsevier, 2021
Nyckelord
3D printing, 3D printed drug products, Printing medicines and pharmaceuticals, Pressure Assisted Microsyringe, Oral drug delivery films, Rheology
Nationell ämneskategori
Reglerteknik Annan materialteknik Annan medicinteknik
Forskningsämne
Materialteknik; Reglerteknik; Medicinsk teknik
Identifikatorer
urn:nbn:se:ltu:diva-82638 (URN)10.1016/j.ijpharm.2021.120197 (DOI)000615977600003 ()33486041 (PubMedID)2-s2.0-85099807137 (Scopus ID)
Forskningsfinansiär
Kempestiftelserna, SMK-1640ÅForsk (Ångpanneföreningens Forskningsstiftelse), 18-459
Anmärkning

Validerad;2021;Nivå 2;2021-02-04 (alebob)

Tillgänglig från: 2021-01-26 Skapad: 2021-01-26 Senast uppdaterad: 2021-04-29Bibliografiskt granskad
Organisationer
Identifikatorer
ORCID-id: ORCID iD iconorcid.org/0000-0002-4628-3857

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