A nanotechnological approach to the enhancement of drug delivery systems for photodynamic therapy
Main Researcher
Prof. Dr. Moustafa Moustafa Mohamed
Duration
. . ~ . .
Sponsoring Foundation
Alexandria University Research Fund (AURF ), Research Enhancement Program (ALEX REP)
Amount of Fund
--
Photodynamic
therapy (PDT) and photodynamic antimicrobial chemotherapy (PACT) are treatment
modalities that are based on the ability of photoactive compounds or
photosensitizers (PS) which under illumination with visible light produce reactive
oxygen species (ROS) leading to cell death. PDT is used clinically for various
neoplastic and non-neoplastic conditions using licensed PSs. In photodynamic
antimicrobial chemotherapy, ROS allow non-specific attack at the microbial
level producing a broad spectrum antibacterial activity regardless of the
conventional drug-resistance status as well as antifungal and antiviral
activity. Moreover, ROS are active against the biofilm structure itself causing
general oxidative breakdown alongside microbial killing. PACT is proposed as a
potential, low-cost approach to the treatment of locally occurring infection.
Limitations
of both anti-cancer PDT and antimicrobial PACT include mainly poor solubility
and permeability of PSs, non selective accumulation at the target site and
sub-optimal selectivity, which present a formulation challenge.Such limitations could be overcome by drug
delivery strategies, particularly at the nano-scale.
Scope of the project: To apply a nanotechnological approach to the enhancement of PDT
and PACT. This is of great scientific and practical importance in view of the
advantage of PDT as more effective and less destructive anti-cancer therapy
compared to surgery, chemotherapy and radiotherapy, particularly in immunocompromised
patients and the
cost/effectiveness of local infections, even those caused by resistant
microbial strains.
Objective: To develop nano-scale carriers for the
controlled delivery of photosensitizers and/or anti-cancer or antimicrobial
chemotherapeutic agents in order to enhance the effectiveness of PDT and
PACT.
Materials:
Polymers
with different physico-chemical properties will be used for the development of
drug-loaded nanocarriers and nanofibres for PDT and PACT respectively. These
will be assessed both in vitro and in vivo.
Expected
outcomes: Application of nanotechnology to the enhancement of cost effective
alternative treatment modalities to improve the potential therapeutic outcomes
and quality of life of a large number of patients