COMPOSITIONS AND METHODS FOR THE TREATMENT AND PROPHYLAXIS OF SURGICAL SITE INFECTIONS
The present invention provides methods for preventing, inhibiting or treating a surgical site infection associated with a surgical operation comprising the step of applying to the surgical site a biocompatible, biodegradable substrate being impregnated and/or having its surface coated fully or partially with a matrix composition which provides local controlled and prolonged release of at least one pharmaceutically active agent at the surgical site.
1 . A method for prophylaxis of a soft-tissue incision site infection associated with a cardiac surgery, wherein the method comprises:
administering directly to the soft-tissue incision site, β-tricalcium phosphate (β-TCP) particles, impregnated or having their surface coated fully or partially with a matrix composition,
wherein the matrix composition comprises:
(a) a biodegradable polymer;
(b) a first lipid component comprising at least one sterol, wherein the at least one sterol is non-covalently associated with the biodegradable polymer;
(c) a second lipid component comprising at least one phospholipid having fatty acid moieties of at least 12 carbons; and
(d) an antibiotic agent.
2 . The method according to claim 1 , wherein the cardiac surgery is an open cardiac surgery.
3 . The method according to claim 1 , wherein the 3-TCP particles having an average particle size of less than 200 microns (μm).
4 . The method according to claim 3 , wherein the average particle size is from 50 μm to 150 μm.
5 . The method according to claim 1 , wherein a majority of the particles are spherical, spheroidal, or any combination thereof.
6 . The method according to claim 1 , wherein the phospholipid is selected from a phosphatidylcholine or a combination of phosphatidylcholines having fatty acid moieties having at least 14 carbons.
7 . The method according to claim 6 , wherein the fatty acid moieties comprise 14 carbons to 18 carbons.
8 . The method according to claim 1 , wherein the biodegradable polymer comprises a polyester selected from the group consisting of PLA (polylactic acid), PGA (poly glycolic acid), PLGA (Poly (lactic co glycolic acid), and any combinations thereof.
9 . The method according to claim 1 , wherein the antibiotic agent is selected from the group consisting of penicillin antibiotics, cephem antibiotics, macrolide antibiotics, tetracycline antibiotics, fosfomycin antibiotics, aminoglycoside antibiotics, quinolone antibiotics, and any combinations thereof.
10 . The method according to claim 9 , wherein the antibiotic agent is a tetracycline antibiotic.
11 . The method according to claim 10 , wherein the tetracycline antibiotic is selected from doxycycline or doxycycline hyclate.
12 . The method according to claim 1 , wherein the matrix composition further comprises a pharmaceutically active agent selected from the group consisting of: an antibiotic agent, an antiseptic agent, an anti-inflammatory agent, an anti-fungal agent, and any combinations thereof.
13 . The method according to claim 1 , wherein the at least one sterol in the matrix composition comprises a cholesterol.
14 . The method according to claim 1 , wherein when the coated or impregnated 3-TCP is maintained in an aqueous environment, the matrix composition provides sustained release of said antibiotic agent, wherein at least 30% of the antibiotic agent is released from the composition at zero-order kinetics.
15 . The method according to claim 1 , wherein the matrix composition comprises:
(a) 10-30% w/w of a biodegradable polymer by weight of the matrix composition;
(b) 5-30% w/w of a first lipid component by weight of the matrix composition;
(c) 40-75% w/w of a second lipid component by weight of the matrix composition; and
(d) 1-20% w/w of antibiotic agent by weight of the matrix composition.
16 . The method according to claim 1 , wherein the coated 3-TCP particles comprise between about 60-90% (w/w) of 3-TCP and 10-40% (w/w) of the matrix composition.
17 . The method according to claim 1 , wherein the infection is caused by hospital acquired resistant bacteria.
18 . The method according to claim 17 , wherein the hospital acquired resistant bacteria include Methicillin-resistant S. aureus (MRSA).
19 . The method according to claim 1 , wherein the coated 3-TCP is formulated as a paste prior to application of the coated 3-TCP particles to the soft-tissue incision site.