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Volume10, Issue 12 (Suppl)

J Proteomics Bioinform, an open access journal

ISSN: 0974-276X

Page 62

conferenceseries

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World Biomarkers & Pharma Biotech 2017

December 07-09, 2017

December 07-09, 2017 | Madrid, Spain

&

20

th

International Conference on

PHARMACEUTICAL BIOTECHNOLOGY

9

th

WORLD BIOMARKERS CONGRESS

JOINT EVENT ON

Surface charge engineering of nitric oxide-releasing polymeric nanoparticles: Adhesion and anti-

biofilm efficacy against wound infection associated MRSA biofilm in db/db mice

Nurhasni Hasan

Pusan National University, South Korea

B

iofilm-associated wound infections have been considered a life-threatening infection that affects millions of people each

year and are among the major cause of infectious disease-related mortality and morbidity worldwide. Bacterial biofilms

protect bacteria from host immune responses and promote strong resistance to antibiotic treatment which leads to impaired

wound healing, hospitalization and amputation particularly in chronic wound such as diabetic foot ulcer. Recently, nitric oxide

(NO) has emerged as novel agent in biofilm dispersal and accelerates wound healing. In this study, we investigated the potency

of positively charge NO-releasing PLGA/PEI nanoparticles (NO/PPNPs) for adhesion on biofilm surface that elevate biofilm

dispersal and wound healing efficacy. Poly (lactic-co-glycolic acid) (PLGA) were used to incorporate polyethyleneimine (PEI)/

NO adduct (PEI/NONOate) by an oil-in-water (O/W) emulsion evaporation method to form NO/PPNPs. Adhesion of NO/

PPNPs on bacterial biofilm and the progress of

in vivo

biofilm dispersal were performed in biofilm wound and characterized

by 3D confocal microscopy.

In vivo

biofilm was prepared by inoculating Methicillin-Resistant Staphylococcus aureus (MRSA)

suspension on the surface of wound in db/db mouse (type-2 diabetic). Photographs of the wounds were taken to observe

the gross visual wound healing. Furthermore, histological analysis was performed with H&E and Masson trichrome stain

to observe the skin morphological and collagen deposition, respectively. Positively charged of NO/PPNPs facilitated the

electrostatic binding to the negatively charged biofilm matrix, thereby increasing the biofilm dispersal by NO released from

NO/PPNPs. NO/PPNPs treatment a biofilm-challenged diabetic mouse accelerated wound healing as compared to untreated

and blank nanoparticles. In addition, histological examination revealed that wounds treated with NO/PPNPs showed increased

numbers of fibroblast-like and collagen deposition with healed skin structures close to the normal healthy epidermis. Thus, the

NO-releasing polymeric nanoparticles investigated in this study could be a promising approach for the treatment of biofilm-

challenged chronic wounds and various skin infections.

Recent Publications:

1. H Nurhasni, J Cao, M Choi, I Kim, B L Lee, Y Jung, J W Yoo (2015) Nitric oxide-releasing poly (lactic-co-glycolic

acid)-polyethylenimine nanoparticles for prolonged nitric oxide release, antibacterial efficacy, and

in vivo

wound

healing activity, International journal of nanomedicine. 10: 3065.

2. J S Choi, J Cao, M Naeem, J Noh, N Hasan, H K Choi, J W Yoo (2014) Size-controlled biodegradable nanoparticles:

Preparation and size-dependent cellular uptake and tumor cell growth inhibition, Colloids and Surfaces B:

Biointerfaces.122: 545-551.

3. J O Kim, J K Noh, R K Thapa, N Hasan, M Choi, J H Kim, J H Lee, S K Ku and J W Yoo (2015) Nitric oxide-releasing

chitosan film for enhanced antibacterial and

in vivo

wound-healing efficacy, International journal of biological

macromolecules. 79: 217-225.

4. J W Yoo, J S Lee, C H Lee (2010) Characterization of nitric oxide‐releasing microparticles for the mucosal delivery,

Journal of Biomedical Materials Research Part A. 92: 1233-1243.

5. J W Yoo, D J Irvine, D E Discher and S Mitragotri (2011) Bio-inspired, bioengineered and biomimetic drug delivery

carriers, Nature reviews. Drug discovery. 10: 521.

hasni1986.nh@gmail.com

Nurhasni Hasan, J Proteomics Bioinform 2017, 10:12(Suppl)

DOI: 10.4172/0974-276X-C1-110