Methods and compositions for disrupting biofilm utilizing chitosan-derivative compounds
Described herein are methods of disrupting (e.g., reducing the viscosity of, or dissolving) a preformed biofilm in a subject, the method comprising: administering to the subject an effective amount of a composition comprising a soluble chitosan or derivatized chitosan wherein the soluble chitosan or derivatized chitosan when administered contacts the preformed biofilm, thereby disrupting (e.g., reducing the viscosity of, or dissolving) the preformed biofilm.
1 . A method of disrupting a preformed biofilm in a subject infected with bacteria selected from the group consisting of Burkholderia cepacia genomovar cenocepacia, Burkholderia cepacia genomovar dolosa, Burkholderia cepacia complex, Staphylococcus aureus, Pseudomonas aeruginosa, Acinetobacter baumanii, Streptococcus pneumoniae , and Klebsiella pneumoniae , the method comprising:
administering to the subject by inhalation a therapeutically effective amount of a composition comprising a derivatized chitosan, wherein the derivatized chitosan comprises a chitosan of the following formula (I):
wherein:
n is an integer between 20 and 6000; and
each R 1 is independently selected for each occurrence from hydrogen, acetyl, and a group of formula (II): wherein formula (II) is selected from
wherein at least 25% of R 1 substituents are H, at least 1% of R 1 substituents are acetyl, and at least 4-30% of R 1 substituents are a group of formula (II), the molecular weight of the derivatized chitosan is between 10,000 and 150,000 Da, and the polydispersity index (PDI) of the derivatized chitosan is between 1.5 and 2.5, wherein, upon administration, the composition disrupts the preformed biofilm in the respiratory system of the subject and reduces the viscosity of sputum in the respiratory system of the subject relative to the sputum prior to administration of the composition.
2 . The method of claim 1 , wherein the PDI of the derivatized chitosan is between 1.5 and 2.3.
3 . The method of claim 1 , wherein the PDI of the derivatized chitosan is between 1.5 and 2.0.
4 . The method of claim 1 , wherein the method reduces the viscosity of the sputum by at least 50% compared to the sputum that has not been contacted with the composition.
5 . The method of claim 1 , wherein the method reduces the viscosity of the sputum by at least 80% compared to the sputum that has not been contacted with the composition.
6 . The method of claim 1 , wherein the method increases the pourability of sputum compared to the sputum that has not been contacted with the composition.
7 . The method of claim 1 , wherein the derivatized chitosan is present in the composition at a concentration of about 10 to 250 μg/mL.
8 . The method of claim 1 , wherein the biofilm is partially dissolved compared to the biofilm that has not been contacted with the composition.
9 . The method of claim 1 , wherein the biofilm is in the respiratory system.
10 . The method of claim 1 , wherein the subject has cystic fibrosis.
11 . The method of claim 1 , wherein the derivatized chitosan is soluble in aqueous solution from about pH 6.8 to about pH 7.4.
12 . The method of claim 1 , wherein the chitosan is functionalized at between 20% and 30%.
13 . The method of claim 1 , wherein the degree of deacetylation (% DDA) of the derivatized chitosan is between 75% and 95%.
14 . The method of claim 1 , wherein the therapeutically effective amount is from about 5 to 500 μg/mL.
15 . The method of claim 1 , further comprising administering an antibiotic, anti-inflammatory, or mucolytic compound to the subject in conjunction with, prior to, or subsequent to the administration of the composition.
16 . The method of claim 1 , wherein the bacteria are multidrug resistant.
17 . The method of claim 1 , wherein between 25-95% of R 1 substituents are hydrogen.
18 . The method of claim 1 , wherein between 1-50% of R 1 substituents are acetyl.
19 . The method of claim 1 , wherein 55-90% of R 1 substituents are hydrogen, 4-20% of R 1 substituents are acetyl, and 4-30% of R 1 substituents are a group of formula (II).