Propylene glycol liposomes for improved delivery of vancomycin to biofilms on abiotic surfaces
Gresha, A., Ramadan, A., Kassem, M., Khallafallah, N. (2024). Propylene glycol liposomes for improved delivery of vancomycin to biofilms on abiotic surfaces. EKB Journal Management System, 1(1), 121-137. doi: 10.21608/japs.2024.255619.1013
Amr E. Gresha; Alyaa A. Ramadan; Mervat A. Kassem; Nawal M. Khallafallah. "Propylene glycol liposomes for improved delivery of vancomycin to biofilms on abiotic surfaces". EKB Journal Management System, 1, 1, 2024, 121-137. doi: 10.21608/japs.2024.255619.1013
Gresha, A., Ramadan, A., Kassem, M., Khallafallah, N. (2024). 'Propylene glycol liposomes for improved delivery of vancomycin to biofilms on abiotic surfaces', EKB Journal Management System, 1(1), pp. 121-137. doi: 10.21608/japs.2024.255619.1013
Gresha, A., Ramadan, A., Kassem, M., Khallafallah, N. Propylene glycol liposomes for improved delivery of vancomycin to biofilms on abiotic surfaces. EKB Journal Management System, 2024; 1(1): 121-137. doi: 10.21608/japs.2024.255619.1013

Propylene glycol liposomes for improved delivery of vancomycin to biofilms on abiotic surfaces

Journal of Advanced Pharmaceutical Sciences
Volume 1, Issue 1, January 2024, Page 121-137  XML PDF (1019.69 K)
Document Type: Original Article
DOI: 10.21608/japs.2024.255619.1013
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Authors
Amr E. Gresha1; Alyaa A. Ramadan email orcid 2; Mervat A. Kassem3; Nawal M. Khallafallah2
1Pharco Pharmaceuticals Co., Alexandria, Egypt
2Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Egypt
3Department of Microbiology and Immunology, Faculty of Pharmacy, Alexandria University
Abstract
Patients fitted with urinary bladder and vascular catheters are subject to bacterial infections and biofilm formation. These infections are mostly caused by coagulase-positive and coagulase-negative staphylococci. Vancomycin (VCM) remains the frontline intravenous antibiotic for the treatment of catheter-related bacteremia. Liposomes are appealing drug carrier systems, especially against colonized microorganisms.
In the present study, VCM-loaded propylene glycol liposomes were prepared by the ethanol injection method The liposomes were characterized pharmaceutically and microbiologically. Pharmaceutical attributes included colloidal properties, entrapment efficiency (EE%), release, and stability. Microbiological tests included the determination of Minimum Inhibitory Concentration (MIC) by two methods, antibiofilm efficacy using the microtiter plate model, including assessment of Minimum Biofilm Inhibitory Concentration (MBIC), Minimum Biofilm Eradicating Concentration (MBEC), and biofilm formation induction by vancomycin sub-minimum inhibitory concentrations. Antibiofilm efficacy was also assessed using the catheter segments model. VCM liposomes showed vesicle size in the nanorange (219.49 ± 20.21 nm), low PDI (0.282 ± 0.044), negative zeta potential (-4.78), and EE% (52.84±1.5%) that proved stable with no drug leakage after 3 months of storage at 4°C. It also showed a slower release profile compared to the free VCM. The antibacterial and antibiofilm efficacy of VCM liposomes compared to free VCM increased by 2–8 folds, calculated from the observed extent of reduction in MIC, MBIC, and MBEC of liposome-loaded VCM compared to free VCM. Results of catheter segment experiments indicated the potential usefulness of VCM liposomes in antibiotic lock solutions for managing biofilms on medical devices and implants.

Highlights
  • Drug delivery strategies have emerged as an effective approach for localized biofilm control on abiotic surfaces such as catheters.
  • Entrapment of antibiotics in liposomes may enhance their antimicrobial and antibiofilm activity.
  • Vancomycin-loaded propylene glycol liposomes were successfully prepared using the ethanol injection method.
  • The developed liposomes showed potential for use as a substitute for VCM in antibiotic lock solutions used to prevent or treat device-related bacteremias.
Keywords
Vancomycin; liposomes; abiotic; biofilm
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