OpenNanoPub Date : 2023-08-31DOI: 10.1016/j.onano.2023.100184
Liu-Ru Fang , Yu-Hua Wang , Zu-Zhao Xiong , Yu-Mei Wang
{"title":"Research progress of nanomaterials in tumor-targeted drug delivery and imaging therapy","authors":"Liu-Ru Fang , Yu-Hua Wang , Zu-Zhao Xiong , Yu-Mei Wang","doi":"10.1016/j.onano.2023.100184","DOIUrl":"10.1016/j.onano.2023.100184","url":null,"abstract":"<div><p>Cancer continues to threaten people's lives and health, and the number of deaths from cancer is very high each year. Traditional treatments such as chemotherapy and surgery are poorly selective and have many side effects. While traditional cancer treatments kill tumor cells, they also damage normal cells and cause a series of toxic side effects. Targeted therapy can compensate for the shortcomings of conventional therapies based on nanomaterials. This paper introduces novel nanomaterials commonly used in tumor-targeted drug delivery as well as imaging therapy, demonstrates the types of active and passive drug delivery systems, and gives examples of research and applications in the past three years. The characteristics of nanomaterials for tumor-targeted therapy and their recent research progress in tumor therapy are summarized. This paper provides theoretical and practical support for nanomaterial-based targeted drug delivery systems and imaging therapy for tumors and provides a reference for the development of nanomaterials for controlled targeted therapy for tumors.</p></div>","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":"14 ","pages":"Article 100184"},"PeriodicalIF":0.0,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46518065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OpenNanoPub Date : 2023-08-30DOI: 10.1016/j.onano.2023.100186
E.T. Aguayo Frías , D. Maza Vega , M.N. Calienni , C. Lillo , D.S. Vazquez , S.d.V. Alonso , J. Montanari
{"title":"Enhanced skin delivery of vismodegib-loaded rigid liposomes combined with ethosomes","authors":"E.T. Aguayo Frías , D. Maza Vega , M.N. Calienni , C. Lillo , D.S. Vazquez , S.d.V. Alonso , J. Montanari","doi":"10.1016/j.onano.2023.100186","DOIUrl":"10.1016/j.onano.2023.100186","url":null,"abstract":"<div><p>Vismodegib, first approved in 2012 for the treatment of basal cell carcinoma, is an inhibitor of the Hedgehog signaling pathway that becomes active in certain tumors. However, its secondary effects after oral administration and systemic distribution are severe. In this study, we loaded vismodegib into conventional liposomes, which are typically unable to penetrate the stratum corneum barrier effectively after topical application. We studied its skin penetration when co-administered with empty ethosomes, aimed at transiently disrupting the skin impermeability.The drug was successfully recovered from the deeper viable epidermal layers in an <em>in vitro</em> model. The preparation method for the liposomal formulation is reproducible and relatively straightforward to scale up. Furthermore, it involves the use of biocompatible lipids, thus avoiding the utilization of potentially risky compounds.</p></div>","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":"14 ","pages":"Article 100186"},"PeriodicalIF":0.0,"publicationDate":"2023-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45563024","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OpenNanoPub Date : 2023-08-30DOI: 10.1016/j.onano.2023.100185
Sumaira Aziz , Rabia Javed , Anna Nowak , Saad Liaqat , Zia Ul Haq Khan , Naveed Ahmad , Mateusz Dulski , Krzysztof Matus , Pervaiz Ahmad , Nawshad Muhammad
{"title":"Effects of TiO2, Ag-TiO2, and Cu-TiO2 nanoparticles on mechanical and anticariogenic properties of conventional pit and fissure sealants","authors":"Sumaira Aziz , Rabia Javed , Anna Nowak , Saad Liaqat , Zia Ul Haq Khan , Naveed Ahmad , Mateusz Dulski , Krzysztof Matus , Pervaiz Ahmad , Nawshad Muhammad","doi":"10.1016/j.onano.2023.100185","DOIUrl":"10.1016/j.onano.2023.100185","url":null,"abstract":"<div><p>The objective of this study was to determine the effects of TiO<sub>2</sub>, Ag-TiO<sub>2,</sub> and Cu-TiO<sub>2</sub> nanoparticles (NPs) addition on the mechanical and antibacterial properties of resin-based sealants. TiO<sub>2</sub>, Ag-TiO<sub>2,</sub> and Cu-TiO<sub>2</sub> NPs were characterized with FTIR, Raman, SEM-EDX, TEM, XPS, and XRD, and evaluated for cytotoxicity study. After characterization, the nanoparticles were mixed with commercial pit and fissure sealants (PAFS) in ratios of 1 and 2%. A total of 7 groups were made, control group (PAFS only) and experimental groups (1%-2% TiO<sub>2</sub>, 1%-2% Ag-TiO<sub>2,</sub> and 1%-2% Cu-TiO<sub>2</sub>). ISO standards were adopted to prepare samples for mechanical properties, i.e., compressive strength (CS), flexural strength (FS), and Vickers hardness evaluation. Samples were tested against <em>Streptococcus mutans</em> through an agar well diffusion test. The CS, FS, and Vickers hardness were increased for the Cu-TiO<sub>2</sub> group with respect to Ag-TiO<sub>2</sub> but values were less compared to TiO<sub>2</sub> groups. The highest flow rate was measured in the control group which was 8.16±0.06 mm and 9.17±0.1 mm after 3 and 10 mins respectively. In the agar well diffusion test, the control group showed no zone of inhibition, and the lowest zone of bacterial inhibition was found in PAFS with 1% TiO<sub>2</sub> NPs group (13.3 ± 1.5 mm) while the highest was found in PAFS with 2% Ag-TiO<sub>2</sub> NPs (21.8 ± 1.7 mm). Cu-doped TiO<sub>2</sub> NPs showed more biocompatibility as compared to Ag-doped TiO<sub>2</sub>. The outcomes were statistically significant for all the mechanical tests and agar well diffusion antibacterial test as the p-value ≤0.05 while for the cytotoxicity test, the p-value >0.05. The TiO<sub>2</sub> addition generally improved both the mechanical and antibacterial properties of pit and fissure sealant.</p></div>","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":"14 ","pages":"Article 100185"},"PeriodicalIF":0.0,"publicationDate":"2023-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43569436","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Drug delivery systems of gefitinib for improved cancer therapy: A review","authors":"Deepak Nagdiya , Manish Kumar , Sanchit Arora , Tania Bajaj , Sima Kujur , Prinsy Rana , Arun Kumar , Arti Singh , Charan Singh","doi":"10.1016/j.onano.2023.100183","DOIUrl":"10.1016/j.onano.2023.100183","url":null,"abstract":"<div><p>Lung cancer is an uncontrolled and abnormal mass of growing cells with the highest mortality rate in the world. Progressive lung cancer shows a robust resistance to cancer therapy; today no acceptable therapeutic results are achieved with drugs. Gefitinib is an epidermal growth factor receptor tyrosine kinase inhibitor and blocks the proliferation of downstream signals that prevent cancer cells from proliferating by inhibiting tyrosine phosphorylation of the epidermal growth factor receptor. It also increases survival rates in patients with progressive lung cancer. Gefitinib belongs to the BCS class II drugs and due to its low bioavailability; its clinical use has been severely restricted. In recent years, several research papers have been published on the use of nanoparticles to increase therapeutic efficacy and drug targeting in lung cancer. Furthermore, to enhance the therapeutic efficacy of gefitinib, nanoparticles have been extensively studied and several nanoparticles including polymers, liposomes, solid lipid nanoparticles, nanostructured lipid carriers, nano cells, albumin, and silica nanoparticles have been developed for the treatment of lung cancer. All of these nanocarriers have improved targeted gefitinib treatment of lung cancer and improved nanomedicines for lung cancer treatment. This article provides an overview of various nanotechnology-based carrier systems of gefitinib such as polymeric, lipidic, albumin, and silica nanoparticles for lung cancer therapy. It also discusses the targeted and responsive delivery of gefitinib along with a combination strategy for better therapeutic efficacy. We believe that this manuscript will bring important information for formulation scientists to overcome the biopharmaceutical challenges associated with gefitinib for better clinical outcomes.</p></div>","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":"14 ","pages":"Article 100183"},"PeriodicalIF":0.0,"publicationDate":"2023-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47560230","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OpenNanoPub Date : 2023-08-01DOI: 10.1016/j.onano.2023.100181
Dinh-Toi Chu, Hue Vu Thi, Tiep Tien Nguyen, Thuy-Duong Vu, Yen Vy Nguyen Thi, I. Mani, Nisarg Gohil, G. Bhattacharjee, Suresh Ramakrisha, Vijai Singh
{"title":"Nanotechnology and nucleic acid nanoparticles for metabolic disorders","authors":"Dinh-Toi Chu, Hue Vu Thi, Tiep Tien Nguyen, Thuy-Duong Vu, Yen Vy Nguyen Thi, I. Mani, Nisarg Gohil, G. Bhattacharjee, Suresh Ramakrisha, Vijai Singh","doi":"10.1016/j.onano.2023.100181","DOIUrl":"https://doi.org/10.1016/j.onano.2023.100181","url":null,"abstract":"","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44996978","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OpenNanoPub Date : 2023-07-01DOI: 10.1016/j.onano.2023.100146
Deepak Gupta , Indrajit Roy , Sona Gandhi
{"title":"Metallic nanoparticles for CT-guided imaging of tumors and their therapeutic applications","authors":"Deepak Gupta , Indrajit Roy , Sona Gandhi","doi":"10.1016/j.onano.2023.100146","DOIUrl":"10.1016/j.onano.2023.100146","url":null,"abstract":"<div><p>Nanoparticles (NPs) serve as the contrasting agent in the computed tomography (CT) guided interventional devices and processes. The high contrast imaging of the patient is critical for accurate and early diagnosis, and thereafter the elimination of the abnormality. A high contrast CT scan helps in the diagnosis of blood clots, broken bones, carcinogenic tumors, infections, internal injuries and bleeding, and cardiovascular diseases. Thereafter it helps in the determination of the precise location of surgery, biopsy, and monitoring conditions after surgery. Besides iodine, today radiologists are interested in high atomic number NPs like gold, tantalum, bismuth, silver, etc. The advancement in NP-based CT-guided imaging for a specific target is highly desirable for effective intervention processes like drainage by catheter, needle insertion, etc. In computed tomography (CT) guided interventional devices and procedures, NPs are known to act as contrasting agents. High-contrast imaging of the patient is essential for an accurate and prompt diagnosis, followed by the treatment of the diseased site. Blood clots, shattered bones, cancerous tumors, infections, internal injuries and bleeding, and cardiovascular disorders can be easily diagnosed with the use of a CT scan with high contrast. In addition, it aids in determining the precise surgical site, conducting biopsies, and monitoring postoperative conditions. Iodine-based contrast agents have been the conventional choice, but lately, radiologists are also interested in NPs with a high atomic number, such as gold, tantalum, bismuth, silver, etc. This review talks about recent research on metallic NPs and the usage of their conjugates for CT imaging of tumors, special attention has been given to gold NPs.</p></div>","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":"12 ","pages":"Article 100146"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43248232","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OpenNanoPub Date : 2023-07-01DOI: 10.1016/j.onano.2023.100149
Andari Sarasati , Hevi Wihadmadyatami , Ika Dewi Ana
{"title":"Carbonate apatite nanoparticles: A novel nano-adjuvant for oral mucosal vaccines and immunomodulator","authors":"Andari Sarasati , Hevi Wihadmadyatami , Ika Dewi Ana","doi":"10.1016/j.onano.2023.100149","DOIUrl":"10.1016/j.onano.2023.100149","url":null,"abstract":"<div><p>Vaccines manufacture and enhancement for preventing infection and promoting quality of life are of great concern worldwide. For vaccine enhancement, to date, only limited adjuvants have been approved globally. One of them is alum, which presents several side effects and limitations. Related to vaccine administration, mucosal vaccination is a promising method since it can induce both mucosal and systemic immunity since oral mucosa is the most exposed site of the body to various microbes, pathogens, and environmental particles. Consequently, an escalated specific local immunity is required in which stability and integrity of an encapsulated antigen is expected to result in a stable mucosal vaccine to protect the antigens from degradative chemical reactions occurring in the oral cavity and act as immunomodulator. Carbonate apatite (CHA) has been one of the most innovative materials as a newly developed vaccine adjuvant since it can adequately enhance drug and protein stability and delivery in various disease therapies. However, CHA fabrication that meets the parameters for adjuvants and immunomodulators remains challenging. In the form of nanoparticles, CHA is reported to enable targeted delivery of dendritic cells (DC), enhance uptakes, cross presentation, and biodistribution, as well as immune responses. Therefore, the development of nano-CHA-encapsulated vaccine antigens is required to enhance oral mucosal vaccinations and their effectiveness to prevent diseases. This study focuses on factors and strategies that affect the designing, fabrication, and testing of CHA nanoparticles for oral mucosal vaccines, especially in the aspect of physicochemical, immunological, cellular, surface chemistry, and biofunctionalization of the nanoparticle.</p></div>","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":"12 ","pages":"Article 100149"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46960091","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OpenNanoPub Date : 2023-07-01DOI: 10.1016/j.onano.2023.100148
Gastón Franceschinis , Mariana Beverina , Merlina Corleto , Ayelen Morena Sosa , Cristian Lillo , Lucrecia Arias Casará , Silvia del Valle Alonso , Paulo Maffia , Jorge Montanari , Maria Eugenia Tuttolomondo , Maria Natalia Calienni
{"title":"Green-synthesized silver nanoparticles using Aloe maculata extract as antibacterial agent for potential topical application","authors":"Gastón Franceschinis , Mariana Beverina , Merlina Corleto , Ayelen Morena Sosa , Cristian Lillo , Lucrecia Arias Casará , Silvia del Valle Alonso , Paulo Maffia , Jorge Montanari , Maria Eugenia Tuttolomondo , Maria Natalia Calienni","doi":"10.1016/j.onano.2023.100148","DOIUrl":"10.1016/j.onano.2023.100148","url":null,"abstract":"<div><p>Nowadays, antibiotic resistance poses a threat to public health worldwide. For this reason, non-traditional antibacterial products, such as silver nanoparticles (AgNPs), offer an opportunity to address this issue. Although AgNPs have been proven to be effective antimicrobial agents, we studied the antibacterial and antibiofilm effects of two novel AgNPs (AgNP-Aloe-1 and AgNP-Aloe-2) obtained by green synthesis, their cytotoxicity on a cell line derived from human keratinocytes, and their skin penetration. These AgNPs were obtained here for the first time from an <em>Aloe maculata</em> aqueous extract as a reducing and capping agent of Ag(I), with varying the initial silver concentrations (5 and 9 mM of AgNO<sub>3</sub> for AgNP-Aloe-1 and AgNP-Aloe-2, respectively). For all the assessments, these were compared with AgNPs obtained from a traditional chemical method employing hydroxylamine hydrochloride as a reducing agent and AgNO<sub>3</sub> (AgNP–NH<sub>2</sub>OH·HCl). The AgNPs were characterized physicochemically by TEM, DLS, Zeta potential, UV–vis, fluorescence, and Raman spectroscopy. Additionally, the concentration of silver forming AgNPs and the reaction yield were determined. Both green-synthesized AgNPs showed an improvement in the inhibition of bacterial growth after 24 h of incubation for <em>E. coli</em> and <em>S. aureus</em>. AgNP-Aloe-1 presented a MIC 4 times lower for both bacteria compared to AgNP–NH<sub>2</sub>OH·HCl, while AgNP-Aloe-2 presented a MIC 32 and 8 time lower for <em>E. coli</em> and <em>S. aureus</em>, respectively. Moreover, they produced a decrease in the biofilm biomass formation from <em>P. aeruginosa</em> at lower concentrations (6.25 μg/ml for AgNP-Aloe-1 and 1.56 μg/ml for AgNP-Aloe-2) than AgNP-NH<sub>2</sub>OH·HCl which only showed a reduction of 30% at the maximum concentration tested. However, AgNP-Aloe-1 and AgNP-Aloe-2 were less efficient in eradicating pre-formed biofilm. Even though AgNP-Aloe-2 showed a lower reaction yield (31.7%) compared to AgNP-Aloe-1 (68.5%), they showed the best antibacterial activity. On the other hand, green-synthesized AgNPs were mainly retained in the <em>stratum corneum</em> of intact skin and reached lower concentrations in the viable epidermis than AgNP–NH<sub>2</sub>OH·HCl. Moreover, AgNP-Aloe-1 and AgNP-Aloe-2 did not show cytotoxic effects on human keratinocytes at the antibacterial concentrations. Their improved performance and lower skin penetration could be attributed to their physicochemical properties, such as size (10–25 nm), charge (around −10 mV), and shape (tendency towards a spherical shape), but mainly to the presence of phytocompounds from the extract that remained attached to the AgNPs, as observed by Raman spectroscopy and UV–vis. For the reasons mentioned above, these novel AgNPs obtained by a more environmentally friendly method have the potential to be used as antibacterial agents, particularly for topical applications.</p></div>","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":"12 ","pages":"Article 100148"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43695666","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OpenNanoPub Date : 2023-07-01DOI: 10.1016/j.onano.2023.100153
Chan Hee Chon , Ju Hee Kim , Hyunseung On, Jiwoong Choi, Sanghun Lee, Euidon Han
{"title":"A microfluidic application for mass production of drug-loaded polymeric microspheres for a long-acting injectable with IVL-DrugFluidic®, a novel microfluidic microsphere manufacturing platform technology","authors":"Chan Hee Chon , Ju Hee Kim , Hyunseung On, Jiwoong Choi, Sanghun Lee, Euidon Han","doi":"10.1016/j.onano.2023.100153","DOIUrl":"10.1016/j.onano.2023.100153","url":null,"abstract":"<div><p>Long acting injectables (LAIs) using polymeric microspheres has been developed to increase patient compliance and reduce side effects. Among many methods for manufacturing polymeric microspheres, microfluidics technology is known to have excellent characteristics in that the produced polymeric microspheres have perfect spherical shape without surface defect and uniform size, and thus have outstanding efficacy without initial burst. However, the mass production of polymeric microspheres was not realized by the inherent limitation that microfluidics is suitable for small quantity manufacturing. Overcoming such limitations, we could show mass production of finasteride-loaded polymeric microspheres (PLGA 7525) for LAIs using our microfluidic manufacturing platform technology, IVL-DrugFluidic®. The microfluidic channels used in manufacturing were optimized through computational fluid dynamics (CFD) simulation to minimize the flow variation between microchannels and eliminated disturbance outside of microchannels by resistance channels. In addition, the solvent removal was improved by applying the baffle and foam breaker system. Therefore, microspheres were mass-produced in the GMP manufacturing environment in perfect spherical shape, smooth surface, and even size distribution. The encapsulation efficiency was almost 100% and the residual solvent was under the Standard of regulation. In the clinical trial using microspheres mass-produced by IVL-DrugFluidic®, we confirmed that the drug release was stably maintained for a month, the target period without initial burst. It was also confirmed that the drug release by dose of microspheres was uniformly proportional. In conclusion, the microsphere manufacturing platform technology, IVL-DrugFluidic® has been proven to be an appropriate system for mass production of polymeric microspheres optimized for LAIs through physicochemical characteristics and clinical trial.</p></div>","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":"12 ","pages":"Article 100153"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42202654","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OpenNanoPub Date : 2023-07-01DOI: 10.1016/j.onano.2023.100160
Harinash Rao , Pei Pei Chong , Priya Madhavan
{"title":"3D printing of microbots, characterisation, and utilisation in combination with allicin against C. albicans biofilms","authors":"Harinash Rao , Pei Pei Chong , Priya Madhavan","doi":"10.1016/j.onano.2023.100160","DOIUrl":"10.1016/j.onano.2023.100160","url":null,"abstract":"<div><p>A major driving factor for antimicrobial resistance which leads to treatment failure for microbial infections ascribed to <em>C. albicans</em> are the formation of biofilms. 3D printing is a rapidly evolving innovation which could revolutionize drug delivery based on its unprecedented opportunity for targeted and improved delivery. Herein, we designed and 3D printed microbots via two photon-polymerisation. Subsequently, characterisation was performed and the activity of microbots independently and in combination with allicin against <em>C. albicans</em> biofilms were investigated. The microbots independently did not affect <em>C. albicans</em> biofilm formation and adhesion nor was there any significant synergistic interaction between microbots and allicin combination. However, this study has pioneered the utilisation of microbots for microbiological applications such as in combination with an antimicrobial to target biofilms. These prototype microbots will act as a guide for the next generation of microbots which will be functionalised to disrupt biofilms magnetically, enhancing allicin delivery and activity.</p></div>","PeriodicalId":37785,"journal":{"name":"OpenNano","volume":"12 ","pages":"Article 100160"},"PeriodicalIF":0.0,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49052514","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}