A Systematic Review on Antimicrobial Applications of Nanofibres

 

Mansi L. Patil1*, Swati S. Gaikwad2, Harshad S. Kapare3

1Department of Pharmaceutical Chemistry, Dr. D.Y. Patil Institute of Pharmaceutical Science and Research, Pimpri – Pune - 411018, India.

2Department of Pharmaceutics, Nagpur College of Pharmacy, Wanadongri, Hingna Road, Nagpur – 441110.

3Department of Pharmaceutics, Dr. D.Y. Patil Institute of Pharmaceutical Science and Research,

Pimpri – Pune - 411018, India.

*Corresponding Author E-mail: swati.gaikwad05@gmail.com

 

ABSTRACT:

Antibiotics resistance is a global issue causing health threats which is further causing mortality. Several attempts have been reported to overcome these issues. Despite of this, there are several limitations associated with conventional approaches. Nanofiber technique is an exciting area which has attracted many researchers due to its biomedical applicability such as in tissue engineering, drug delivery, and water purification. Antibiotics encapsulation inside the nanofibres gives the ability to destroy drug-resistant bacteria, additionally its large surface area allows for adhesion of cells as well as drugs. The present review focuses on the potential therapeutic applications of nanofibre technology in antimicrobial drug delivery.

 

KEYWORDS: Biomedicine, Drug delivery, Electrospinning, Nanofibres.

 

 


1. INTRODUCTION: 

The invention of antibiotics is the greatest scientific achievement of the 20th century. It has demonstrated outstanding success in both preventing infections during organ transplant heart surgery and treating infectious disorders.Salvarsan was the first antibiotic to be used, and throughout the past century, antibiotic development has seen a significant transformation. With the discovery of penicillin in 1928, the antibiotic golden age began. Apart from their effectiveness, improper antibiotic use has resulted in the emergence of antibiotic resistance.1,2,3. In essence, antibiotic resistance is now a major problem that threatens human health since it increases mortality and makes it more challenging to treat common infectious diseases.

 

The main issue with oral, intravenous, and intramuscular antibiotic administration is that they result in faster drug delivery at the site of action, which may lead to antibiotic resistance and toxicity issues.

 

The main impediment to the healing process is caused by microorganisms such as bacteria and fungi. As a result, a variety of solutions, such as the nanoparticulate system, have been developed to address these issues. Drug-loaded electrospunnanofibres have been used as an alternative to other nanotechnology-based drug delivery methods, such as nanoparticles and nanoemulsions, because of their high drug loading capacity and effective encapsulation.4,5

 

2. NANOFIBRES IN DRUG DELIVERY:

Because of their large surface area, porosity, and small fiber size, nanofibres are excellent materials for drug delivery. Nanofibres provide variety in fibre synthesis, homogeneous drug release at the site of action, and the lightweight fibrous system's flexibility. The solubility of the drug has a significant impact on the adhesion characteristics between the drug and the nanofibres6-10. The type of polymer has a significant impact on the solvent choice. For stable drug release, hydrophobic drugs are typically combined with hydrophobic polymers, whereas hydrophilic drugs are typically combined with hydrophilic polymers11-13. Due to the manufacture of nanofibres with a diameter less than 1 µm, electro spinning techniques have become more and more popular14,15. Numerous benefits, including great therapeutic efficacy at low doses, less toxicity, and minimal side effects, are provided by nanofiber drug delivery systems. Giram et al. (2018) created antimicrobial electrospun nonwoven Eudragit L-100 nanofibrous mats containing Moxifloxacin hydrochloride for quick drug delivery systems and assessed their antibacterial properties. Investigations were also conducted on the morphological, physicochemical, mechanical, and thermal properties. Regarding encapsulation effectiveness and antibacterial potential, positive findings were obtained.

 

Non-fibrous mats were tested for antibacterial activity against the pathogens Staphylococcus aureus and Escherichia coli in both qualitative and quantitative tests. The quantitative antimicrobial assay results revealed that the moxifloxacin hydrochloride-developed mats (EL-100, EL-100 b, and EL-100 c) outperformed the control and EL-100. The agar diffusion method was used for the qualitative analysis. The zone of inhibition expanded as medication concentration increased. As a result, they showed potent antibacterial activity against both gram-positive and gram-negative bacteria. The in vitro cytotoxicity assay was carried out using the MTT test. The mats were found to be cytotoxic and to promote cell proliferation16.

 

With the help of Eudragit S-100 nonwoven fibrous mats, Rade PP et al. (2022) created a metronidazole delivery system with antibacterial activity for therapeutic effect in the colon. Using the electro spinning technique, it was discovered that the average diameters of the manufactured mats fell between 150 and 600nm. ES-100 nonfibrous mats containing 1, 5, 10, and 15% were manufactured. Antibacterial activity against the gram-positive bacteria Staphylococcus aureus and the gram-negative bacteria Escherichia coli was investigated using the agar diffusion method. Metronidazole is a drug that is frequently used to treat infections caused by anaerobic bacteria. On ES-100 nonfibrous mats that were loaded with metronidazole, significant antibacterial activity was observed. As metronidazole concentration increased, the zone of inhibition expanded. Metronidazole was found to be delivered to the target site at a rate of 74% at pH 6.8. Thus, it can be a good approach for antimicrobial study17.

 

Gentamycin is bactericidal when used against bacteria such as E. coli, Staphylococcus aureus, and pseudomonas aeruginosa.18-20. Compared to other aminoglycosides, gentamycin shows a lower rate of resistance21-24. Gentamycin toxicity is associated with its ability to enter cells and interfere with protein synthesis 25-27. Liposomes, a type of lipid-based medication carrier, can be useful28-30. Therefore, gentamycin loaded liposomes can be employed to improve the accumulation of medication at the site of action and can also solve the issue of nephrotoxicity that may emerge due to numerous daily doses31,32.

 

Nelson Monterio (2015) created a gentamycin-loaded liposome on the surface of chitosan nanofibre mesh to demonstrate antibacterial activity. Thiol groups were used to functionalize chitosan nanofiber meshes, and the reaction between the SH groups and maleimide resulted in gentamicin-loaded liposomes being covalently immobilized. Antibacterial activity was tested on Escherichia coli, Staphylococcus aureus, and pseudomonas aeruginosa. The disc diffusion and broth dilution assays were used to assess activity. The results showed that gentamycin inhibited bacterial growth when released from liposomes attached to the surface of electrospun chitosan NFM. Overall, the findings demonstrated that the developed drug delivery system can be used to treat wounds and eradicate pathogens caused by local infection.

 

By utilising the acetic acid to solvent in acid technique, ciprofloxacin was integrated into the polyvinyl pyrrolidone polymer matrix. From the solution, transparent antimicrobial films were created. To create non-transparent nanofiber mats for testing a compound's antibacterial activity, the compounds were electrospun. They employed Bacillus subtilis and E. coli18. A mouse model for in vivo excision skin wound healing confirmed the films' and nanofibres' promising resorptionproperties. Transparent films were found to degrade much more slowly than nanofibers33.

 

All infections can be effectively blocked by the skin. It is essential for both maintaining body temperature and acting as protection34,35. The main issue that arises when the skin is wounded is bacterial infection36. The intricacy of the healing process for wounds is increased by bacterial infections37. Electrospunnanofibres have been found to effectively aid in wound healing. In the current study, ciprofloxacin and silver nanoparticles were placed into an electrospinning process to create janus wound dressings made of PVP and ethyl cellulose. S. aureus and E. coli microorganisms were examined for their potential antibacterial properties. Overall, janusfibres had a potent and long-lasting antibacterial activity, suggesting synergistic actions of both silver and ciprofloxacin.

 

3. NANOFIBRES IN TISSUE ENGINEERING:

Nanofibres with a high surface area to volume ratio have received a lot of attention in tissue engineering, drug delivery, and other biomedical devices38. Surface functionalized nanofibres have a lot of potential in tissue engineering applications like bone tissue engineering, cartilage tissue engineering, osteochondrial tissue engineering, and so on39.

 

Prior to the beginning of human clinical trials, the rat calvarial size underwent in vivo testing, which produced scaffolds and established the gold standards in the preclinical setting40. The in vivo conditions reflect the scaffolds actual performance in terms of cellular response, cellular rejection, and the production of new tissue41.

 

Biocompatible and biodegradable polymers of natural and synthetic origin, such as chitosan, collagen, and gelatin, which have the capacity to boost in-vitro cell growth, are being developed as new scaffolds for tissue engineering42. Due to developing technologies that will require biomaterials that are physically and chemically robust, conducting polymers are of great interest in tissue engineering applications. They aid in the growth of tissues and are electrically conductive, making them capable of initiating or stimulating specific cell processes43. Polyaniline (PANI) and polypyrrole (PPy), which have the ability to transport currents in biological environments, are being researched for their potential to locally deliver electrical stimulation to wounded tissue to speed wound healing44-45. Considering these qualities into account By using an electrospinning technique, Nikolaidis M. G et al. (2010) created blends of poly (lactic acid) and poly(aniline-co-3-aminobenzoic acid) that had been doped with HCL and tested for antimicrobial properties. S. aureus was the microbe utilised in the study.

 

BacLight was used to research the antibacterial impact of nanofibres on the viability of bacteria. Results of the study showed that there were much less bacteria on the functionalized nanofibers (31%) than on glass or poly (lactic acid), demonstrating their antibacterial potential. The created nanofibres encouraged healthy cell growth and exclusively eliminated harmful bacteria, making them ideal for use in antimicrobial wound dressings. Wound infection is a big worry for those whose immune systems are weakened. Delays in wound closure are brought on by an increase in wound infection46,47. It is urgently necessary to develop methods for minimising wound infection and further limiting the ability of bacteria to evolve into more drug resistant strains due to the rise in multi-drug resistant bacteria.

 

Bringing silver ions to the area of action is one approach that could be used in this situation48. The wound site receives 3–4 topically administered applications of silver nitrate every day49. Additionally, 1% cream or suspension of silver sulfadiazine is used to burns and wounds50. Both of these methods, however, do not continuously release silver ions, therefore frequent reapplication of the compound to the wound site is necessary51.

 

Silver nanoparticles with a high surface area that permit a wide release of silver ions are thus being investigated for use in wound dressings as a means of preventing bacterial infection.

 

The cytotoxic effects of the dressings on the host cells must be taken into account when assessing the antibacterial capabilities52,53.

 

However, epidermal keratinocytes and dermal fibroblast cells of the skin are shown to be damaged upon exposure to high concentrations of silver ions, despite the fact that the low toxicity of silver ions to mammalian cells is observed in some mammalian cells54.

 

The study report investigated the antibacterial effectiveness and cytotoxicity of silver-based wound dressings, as well as high surface area metallic silver in the form of extremely porous silver nanoparticles incorporated within poly-lactic acid nanofibrous dressings.55,56.

 

Staphylococcus aureus and human epidermal keratinocyte co-culture systems were developed for the simultaneous evaluation of antibacterial and cytotoxic effectiveness. For a better understanding of the outcomes of the co-culture system, experiments using S. aureus or human epidermal keratinocytes have been published. Compared to pure PLA control, antibacterial activity indicated that S.aureus bacteria on silver ions grew more slowly.

 

Although the initial concentration of silver ions within the nanoparticles might be raised, it is not advised unless the wound dressings are extremely diseased. It was found that the amount of released silver ions from both scaffolds was insufficient to kill all bacteria in the solution.

 

The outcomes showed that pure PLA, AgNP loaded as well as AgMP loaded nanoparticles inhibited the viability and proliferation of human epidermal keratinocytes. S. aureus bacteria were observed to proliferate less quickly on chemicals put on epidermal keratinocytes than on an acellular scaffold. Therefore, it can be investigated in various wound dressings or skin substitutes57.

 

4. NANOFIBRES IN WATER PURIFICATION:

Bacteria and viruses are the primary causes of drinking water contamination in underdeveloped nations58. There are almost 1.1 billion individuals who lack access to clean water. Chlorine and a membrane-based water filtration system are used to control microbiological infections. However, the growth in infections with heightened resistance has made this strategy less reliable. Biofouling and viral penetration were discovered to be the main sources of the challenges in water treatment59.

 

Reverse osmosis and other high-energy filtration techniques, such as nanofiltration, have been shown to be effective at removing microorganisms. Low pressure membranes with anti-biofouling and antiviral pathogens are utilised, but because filtering uses a lot of energy, they are becoming more and more popular60. The properties of nanofibre filtering media vary in thickness, diameter, and customised pore size, depending on the polymer. Nanobiocides such as metal nanoparticles, antibiotics, and antibacterial agents can be enclosed in dry nanofibres by including them in the polymer solution. The manufacturing of these nanofibres takes place by the electrospinning process61. These factors were taken into consideration by Zodrow K et al. in 2009 when they created antimicrobial nanofibres and described how they may be used to purify water. The successful production of antimicrobial nanofibers depends on the choice of the right surfactants and polymers. Polymer surfactant interactions have a significant impact on the electrospinning process62.

 

Yoon K et al. (2006) developed a new type of high flux UF/NF medium that can replace conventional porous membranes and provide a significantly higher flux rate for water filtration using an electrospunnanofibrous scaffold and a thin top layer of hydrophilic, water-resistant, but water-permeable chitosan coating63.

 

5. CONCLUSION:

Numerous resources are being used to research how nanofibres can be used in biomedicine. As a result, there are now more polymers available to be employed in the electrospinning process to create nanofibers. These biocompatible polymers, each of which has a unique set of features, are encouraging scientists to combine diverse polymers that couldn't normally be electrospun directly. The research published by numerous researchers helps us understand how drugs are released for tissue regeneration and identifies the purpose and size of nanofibres that can be further refined for their use in tissue engineering64. Antimicrobial nanofibres have drawn the attention of numerous researchers for the development of efficient drug delivery systems due to their substantial surface area. Antimicrobial nanofibres have a proven potential use in the filtration of water. Antimicrobial nanofibres have been found to minimise the viral and bacterial load, which automatically lessens the problem of biofouling.

 

6. ACKNOWLEDGEMENT:

The author would like to extend sincere appreciation to Dr.D.Y. Patil Institute of Pharmaceutical science and Research, Pimpri-Pune and Nagpur College of pharmacy, Wanadongri, Hingna road, Nagpur, Maharashtra, India for providing literature survey facility to compile this article.      

 

7. REFERENCES:

1.     Hutchings MI, Truman AW, Wilkinson B. Antibiotics: past, present and future. Current opinion in microbiology. 2019 ;51:72-80.https://doi.org/10.1016/j.mib.2019.10.008

2.     Purohit MC, et.al. Antimicrobial Activity of Synthesized Zinc Oxide Nanoparticles using Ajugabracteosa Leaf Extract. Asian Journal of Pharmaceutical Analysis. 2021; 11(4): 275-0. doi: 10.52711/2231-5675.2021.00047

3.     Karthick, P. Kumaravel, P. Hemalatha, L. Thamaraiselvi. Mechanistic aspects: Biosynthesis of Silver nanoparticles from Proteus mirabilis and its antimicrobial study. Research J. Science and Tech 2013; 5(2): 235-238. https://rjstonline.com/AbstractView.aspx?PID=2013-5-2-1

4.     Ulubayram K, Calamak S, Shahbazi R, Eroglu I. Nanofibers based antibacterial drug design, delivery and applications. Current Pharmaceutical Design. 2015 ; 21(15): 1930-43. DOI: 10.2174/1381612821666150302151804

5.     Hamdan N, Yamin A, Hamid SA, Khodir WK, Guarino V. Functionalized antimicrobial nanofibers: Design criteria and recent advances. Journal of Functional Biomaterials. 2021 ; 12(4):59.DOI: 10.3390/jfb12040059

6.     Lou L, Subbiah S, Smith E, Kendall RJ, Ramkumar SS. Functional PVA/VB2/TiO2 nanofiber webs for controlled drug delivery. ACS Applied Bio Materials. 2019; 2(12): 5916-29. https://doi.org/10.1021/acsabm.9b00726

7.     Saha K, Butola BS, Joshi M. Drug‐loaded polyurethane/clay nanocompositenanofibers for topical drug‐delivery application. Journal of Applied Polymer Science. 2014 May 15;131(10).DOI: 10.1002/app.40230

8.     Bolgen, N.; Vargel, I.; Korkusuz, P.; Menceloglu, Y. Z.; Piskin, E. J. Biomed. Mater. Res. B Appl. Biomater. 2007, 81,530.https://doi.org/10.1002/jbm.b.30694

9.     Prabhakar  C, Bala Krishna K. A Review on Polymeric Nanoparticles. Research J. Pharm. and Tech. 2011; 4(4): 496-498.https://rjptonline.org/HTMLPaper.aspx?Journal=Research%20Journal%20of%20Pharmacy%20and%20Technology;PID=2011-4-4-12

10.   Kushwah P, Mandloi R, Pillai S, Birla N, Sen A. A Review on Role of Nanoparticles in Anticancer Drugs. Res. J. Pharmacognosy and Phytochem. 2020; 12(3): 168-173. https://doi.org/10.5958/0975-4385.2020.00028.X

11.   Huang ZM, He CL, Yang A, Zhang Y, Han XJ, Yin J, Wu Q. Encapsulating drugs in biodegradable ultrafine fibers through co‐axial electrospinning. Journal of Biomedical Materials Research Part A: An Official Journal of The Society for Biomaterials, The Japanese Society for Biomaterials, and The Australian Society for Biomaterials and the Korean Society for Biomaterials. 2006; 77(1): 169-79. DOI: 10.1002/jbm.a.30564

12.   Kim K, Luu YK, Chang C, Fang D, Hsiao BS, Chu B, Hadjiargyrou M. Incorporation and controlled release of a hydrophilic antibiotic using poly (lactide-co-glycolide)-based electrospunnanofibrous scaffolds. Journal of controlled release. 2004; 98(1): 47-56.DOI: 10.1016/j.jconrel.2004.04.009

13.   Jalvandi J, White M, Gao Y, Truong YB, Padhye R, Kyratzis IL. Polyvinyl alcohol composite nanofibres containing conjugated levofloxacin-chitosan for controlled drug release. Materials Science and Engineering: C. 2017; 73: 440-6. DOI: 10.1016/j.msec.2016.12.112

14.   Kim TG, Lee DS, Park TG. Controlled protein release from electrospun biodegradable fiber mesh composed of poly (ɛ-caprolactone) and poly (ethylene oxide). International journal of pharmaceutics. 2007; 338(1-2): 276-83. DOI: 10.1016/j.ijpharm.2007.01.040

15.   Zhou FL, Gong RH. Manufacturing technologies of polymeric nanofibres and nanofibre yarns. Polymer International. 2008; 57(6): 837-45.DOI: 10.1002/pi.2521

16.   Giram PS, Shitole A, Nande SS, Sharma N, Garnaik B. Fast dissolving moxifloxacin hydrochloride antibiotic drug from electrospunEudragit L-100 nonwoven nanofibrous Mats. Materials Science and Engineering: C. 2018; 92: 526-39. DOI: 10.1016/j.msec.2018.06.031

17.   Rade PP, Giram PS, Shitole AA, Sharma N, Garnaik B. Physicochemical and in Vitro Antibacterial Evaluation of Metronidazole Loaded Eudragit S-100 Nanofibrous Mats for the Intestinal Drug Delivery. Advanced Fiber Materials. 2022; 4(1): 76-88. DOI: 10.1007/s42765-021-00090-y

18.   Monteiro N, Martins M, Martins A, Fonseca NA, Moreira JN, Reis RL, Neves NM. Antibacterial activity of chitosan nanofiber meshes with liposomes immobilized releasing gentamicin. Actabiomaterialia. 2015; 18: 196-205. DOI: 10.1016/j.actbio.2015.02.018

19.   Moser A, Stephan R, Corti S, Lehner A. Resistance profiles and genetic diversity of Escherichia coli strains isolated from acute bovine mastitis. Schweizer Archivfür Tierheilkunde. 2013; 155(6): 351-8. DOI: 10.1024/0036-7281/a000470

20.   Rapoport N, Smirnov AI, Pitt WG, Timoshin AA. Bioreduction of tempone and spin-labeled gentamicin by gram-negative bacteria: kinetics and effect of ultrasound. Archives of Biochemistry and Biophysics. 1999; 362(2): 233-41.DOI: 10.1006/abbi.1998.1020

21.   Lan Y, Li W, Jiao Y, Guo R, Zhang Y, Xue W, Zhang Y. Therapeutic efficacy of antibiotic-loaded gelatin microsphere/silk fibroin scaffolds in infected full-thickness burns. Actabiomaterialia. 2014; 10(7): 3167-76. DOI: 10.1016/j.actbio.2014.03.029

22.   Elsner JJ, Shefy‐Peleg A, Zilberman M. Novel biodegradable composite wound dressings with controlled release of antibiotics: microstructure, mechanical and physical properties. Journal of Biomedical Materials Research Part B: Applied Biomaterials. 2010 ; 93(2): 425-35.DOI: 10.1002/jbm.b.31599

23.   Martins A, Araújo JV, Reis RL, Neves NM. Electrospun nanostructured scaffolds for tissue engineering applications.Nanomedicine (Lond). 2007; 2(6): 929-42. DOI: 10.2217/17435889.2.6.929

24.   Chong EJ, Phan TT, Lim IJ, Zhang YZ, Bay BH, Ramakrishna S, Lim CT. Evaluation of electrospun PCL/gelatin nanofibrous scaffold for wound healing and layered dermal reconstitution. Actabiomaterialia. 2007; 3(3): 321-30.DOI: 10.1016/j.actbio.2007.01.002.

25.   Yu LM, Kazazian K, Shoichet MS. Peptide surface modification of methacrylamide chitosan for neural tissue engineering applications. Journal of Biomedical Materials Research Part A. 2007; 82(1): 243-55.DOI: 10.1002/jbm.a.31069

26.   Gubernator J, Drulis-Kawa Z, Dorotkiewicz-Jach A, Doroszkiewicz W, Kozubek A. In vitro antimicrobial activity of liposomes containing ciprofloxacin, meropenem and gentamicin against gram-negative clinical bacterial strains. Letters in Drug Design & Discovery. 2007; 4(4): 297-304. DOI: 10.2174/157018007784620040

27.   Kovács E, Savopol T, Iordache MM, Săplăcan L, Sobaru I, Istrate C, Mingeot-Leclercq MP, Moisescu MG. Interaction of gentamicin polycation with model and cell membranes. Bioelectrochemistry. 2012; 87: 230-5. DOI: 10.1016/j.bioelechem.2012.03.001

28.   Mugabe C, Azghani AO, Omri A. Liposome-mediated gentamicin delivery: development and activity against resistant strains of Pseudomonas aeruginosa isolated from cystic fibrosis patients. Journal of Antimicrobial Chemotherapy. 2005; 55(2): 269-71. DOI: 10.1093/jac/dkh518

29.   Ulbrich W, Lamprecht A. Targeted drug-delivery approaches by nanoparticulate carriers in the therapy of inflammatory diseases. Journal of The Royal Society Interface. 2010 ;7(suppl_1):S55-66. DOI: 10.1098/rsif.2009.0285.focus

30.   Ellbogen MH, Olsen KM, Gentry-Nielsen MJ, Preheim LC. Efficacy of liposome-encapsulated ciprofloxacin compared with ciprofloxacin and ceftriaxone in a rat model of pneumococcal pneumonia. Journal of Antimicrobial Chemotherapy. 2003; 51(1): 83-91.DOI: 10.1093/jac/dkg024

31.   Cordeiro C, Wiseman DJ, Lutwyche P, Uh M, Evans JC, Finlay BB, Webb MS. Antibacterial efficacy of gentamicin encapsulated in pH-sensitive liposomes against an in vivo Salmonella entericaserovartyphimurium intracellular infection model. Antimicrobial agents and Chemotherapy. 2000; 44(3): 533-9. DOI: 10.1128/AAC.44.3.533-539.2000

32.   Drulis-Kawa Z, Gubernator J, Dorotkiewicz-Jach A, Doroszkiewicz W, Kozubek A. A comparison of the in vitro antimicrobial activity of liposomes containing meropenem and gentamicin. Cellular and Molecular Biology Letters. 2006 ; 11(3): 360-75. DOI: 10.2478/s11658-006-0030-6

33.   Contardi M, Heredia-Guerrero JA, Perotto G, Valentini P, Pompa PP, Spanň R, Goldoni L, Bertorelli R, Athanassiou A, Bayer IS. Transparent ciprofloxacin-povidone antibiotic films and nanofiber mats as potential skin and wound care dressings. European Journal of Pharmaceutical Sciences. 2017; 104: 133-44. DOI: 10.1016/j.ejps.2017.03.044

34.   Anand U, Kurup L, Mukherjee S. Deciphering the role of pH in the binding of ciprofloxacin hydrochloride to bovine serum albumin. Physical Chemistry Chemical Physics. 2012; 14(12): 4250-8. DOI: 10.1039/c2cp00001f

35.   Aranaz I, Gutiérrez MC, Yuste L, Rojo F, Ferrer ML, Del Monte F. Controlled formation of the anhydrous polymorph of ciprofloxacin crystals embedded within chitosan scaffolds: Study of the kinetic release dependence on crystal size. Journal of Materials Chemistry. 2009; 19(11): 1576-82. DOI:https://doi.org/10.1039/B813156B

36.   Baker DS, Waldrop B, Arnold J. Compatibility and stability of cefotaxime, vancomycin, and ciprofloxacin in antibiotic lock solutions containing heparin. International Journal of Pharmaceutical Compounding. 2010; 14(4): 346-9. PMID: 23965543.

37.   Bhattacharya S, Sharma DK, Saurabh S, De S, Sain A, Nandi A, Chowdhury A. Plasticization of poly (vinylpyrrolidone) thin films under ambient humidity: Insight from single-molecule tracer diffusion dynamics. The Journal of Physical Chemistry B. 2013; 117(25): 7771-82. DOI: 10.1021/jp401704e

38.   Yang J, Wang K, Yu DG, Yang Y, Bligh SW, Williams GR. Electrospun Janus nanofibers loaded with a drug and inorganic nanoparticles as an effective antibacterial wound dressing. Materials Science and Engineering: C. 2020; 111: 110805.DOI: 10.1016/j.msec.2020.110805

39.   Borges LG, Savi A, Teixeira C, de Oliveira RP, De Camillis ML, Wickert R, Brodt SF, Tonietto TF, Cremonese R, da Silva LS, Gehm F. Mechanical ventilation weaning protocol improves medical adherence and results. Journal of Critical Care. 2017; 41: 296-302.DOI: 10.1016/j.jcrc.2017.07.014

40.   Gol S, Pena RN, Rothschild MF, Tor M, Estany J. A polymorphism in the fatty acid desaturase-2 gene is associated with the arachidonic acid metabolism in pigs. Scientific Reports. 2018; 8(1): 1-9.DOI: 10.1038/s41598-018-32710-w

41.   Loo Y, Wong YC, Cai EZ, Ang CH, Raju A, Lakshmanan A, Koh AG, Zhou HJ, Lim TC, Moochhala SM, Hauser CA. Ultrashort peptide nanofibrous hydrogels for the acceleration of healing of burn wounds. Biomaterials. 2014; 35(17): 4805-14. DOI: 10.1016/j.biomaterials.2014.02.047

42.   Tian H, Tang Z, Zhuang X, Chen X, Jing X. Biodegradable synthetic polymers: Preparation, functionalization and biomedical application. Progress in Polymer Science. 2012; 37(2): 237-80. DOI:10.1016/j.progpolymsci.2011.06.004

43.   Gizdavic‐Nikolaidis M, Ray S, Bennett JR, Easteal AJ, Cooney RP. Electrospun functionalized polyaniline copolymer‐based nanofibers with potential application in tissue engineering. Macromolecular Bioscience. 2010; 10(12): 1424-31. PMID20842683

44.   Zhang YZ, Venugopal J, Huang ZM, Lim CT, Ramakrishna S. Crosslinking of the electrospun gelatin nanofibers. Polymer. 2006; 47(8): 2911-7.https://doi.org/10.1016/j.polymer.2006.02.046

45.   Rho KS, Jeong L, Lee G, Seo BM, Park YJ, Hong SD, Roh S, Cho JJ, Park WH, Min BM. Electrospinning of collagen nanofibers: effects on the behavior of normal human keratinocytes and early-stage wound healing. Biomaterials. 2006; 27(8): 1452-61.DOI: 10.1016/j.biomaterials.2005.08.004

46.   Mo XM, Xu CY, Kotaki ME, Ramakrishna S. Electrospun P (LLA-CL) nanofiber: a biomimetic extracellular matrix for smooth muscle cell and endothelial cell proliferation. Biomaterials. 2004; 25(10): 1883-90. DOI: 10.1016/j.biomaterials.2003.08.042

47.   Di Martino A, Sittinger M, Risbud MV. Chitosan: a versatile biopolymer for orthopaedic tissue-engineering. Biomaterials. 2005; 26(30): 5983-90.DOI: 10.1016/j.biomaterials.2005.03.016

48.   Oren R, Sfez R, Korbakov N, Shabtai K, Cohen A, Erez H, Dormann A, Cohen H, Shappir J, Spira ME, Yitzchaik S. Electrically conductive 2D-PAN-containing surfaces as a culturing substrate for neurons. Journal of Biomaterials Science, Polymer Edition. 2004; 15(11): 1355-74. DOI: 10.1163/1568562042368077

49.   Hannon GJ. RNA interference. nature. 2002 Jul;418(6894):244-51.DOI: 10.1038/418244a

50.   Pavlovich AL, Manivannan S, Nelson CM. Adipose stroma induces branching morphogenesis of engineered epithelial tubules. Tissue Engineering Part A. 2010; 16(12): 3719-26. DOI: 10.1089/ten.TEA.2009.0836

51.   Madsen SM, Westh H, Danielsen L, Rosdahl VT. Bacterial colonization and healing of venous leg ulcers. Apmis. 1996; 104(7‐8): 895-9. DOI: 10.1111/j.1699-0463.1996.tb04955.x

52.   Robson MC. Wound infection: a failure of wound healing caused by an imbalance of bacteria. Surgical Clinics of North America. 1997; 77(3): 637-50.DOI: 10.1016/s0039-6109(05)70572-7

53.   Wright JB. The comparative efficacy of two antimicrobial barrier dressings: in-vitro examination of two controlled release silver dressings. Wounds. 1998; 10: 179-88.

54.   Klasen HJ. A historical review of the use of silver in the treatment of burns. II. Renewed interest for silver. Burns. 2000; 26(2): 131-8. DOI: 10.1016/s0305-4179(99)00116-3

55.   Fox CL. Silver sulfadiazine—a new topical therapy for pseudomonas in burns: therapy of pseudomonas infection in burns. Archives of Surgery. 1968; 96(2): 184-8. DOI: 10.1001/archsurg.1968.01330200022004

56.   Wilkinson LJ, White RJ, Chipman JK. Silver and nanoparticles of silver in wound dressings: a review of efficacy and safety. Journal of Wound Care. 2011; 20(11): 543-9. DOI: 10.12968/jowc.2011.20.11.543

57.   Kirsner RS. Matrix metalloproteinases in normal and impaired wound healing: a potential role of nanocrystalline silver. Wounds, C. 2002;13(3):4-12.

58.   Wright JB, Lam K, Buret AG, Olson ME, Burrell RE. Early healing events in a porcine model of contaminated wounds: effects of nanocrystalline silver on matrix metalloproteinases, cell apoptosis, and healing. Wound Repair and Regeneration. 2002; 10(3): 141-51. DOI: 10.1046/j.1524-475x.2002.10308.x

59.   Lansdown AB. Silver in health care: antimicrobial effects and safety in use. Biofunctional Textiles and The Skin. 2006; 33: 17-34. DOI: 10.1159/000093928

60.   Ahmed FE, Lalia BS, Hashaikeh R. A review on electrospinning for membrane fabrication: Challenges and applications. Desalination. 2015; 356: 15-30. https://doi.org/10.1016/j.desal.2014.09.033.

61.   Al-Attabi R, Rodriguez-Andres J, Schütz JA, Bechelany M, Des Ligneris E, Chen X, Kong L, Morsi YS, Dumee LF. Catalytic electrospunnano-composite membranes for virus capture and remediation. Separation and Purification Technology. 2019; 229: 115806.DOI: 10.1002/adem.201700572

62.   Barhate RS, Ramakrishna S. Nanofibrous filtering media: filtration problems and solutions from tiny materials. Journal of Membrane Science. 2007; 296(1-2): 1-8. https://doi.org/10.1016/j.memsci.2007.03.038

63.   Frenot A, Chronakis IS. Polymer nanofibers assembled by electrospinning. Current opinion in colloid & interface science. 2003; 8(1): 64-75. http://dx.doi.org/10.1016/S1359-0294(03)00004-9

64.   Yoon K, Kim K, Wang X, Fang D, Hsiao BS, Chu B. High flux ultrafiltration membranes based on electrospunnanofibrous PAN scaffolds and chitosan coating. Polymer. 2006; 47(7): 2434-41. DOI: 10.1016/j.polymer.2006.01.042

65.   MullaTS.,Thorat MS, Rayate Y, Nitalikar M . Liposome as a Drug Carrier. Asian J. Res. Pharm. Sci. 2019; 9(2): 141-147. DOI: 10.5958/2231-5659.2019.00021.3

 

 

 

 

 

Received on 31.01.2023           Modified on 17.07.2023

Accepted on 04.12.2023          © RJPT All right reserved

Research J. Pharm. and Tech 2024; 17(1):427-432.

DOI: 10.52711/0974-360X.2024.00067