Microfluidic preparation of fluorocarbon nanodroplets

Patent metadata

Field	Value
Publication number	US-2023404920-A1
Application number	US-202118036018-A
Country	US
Kind code	A1
Filing date	Nov 11, 2021
Priority date	Nov 11, 2020
Publication date	Dec 21, 2023
Grant date	—

Abstract

The present invention relates to calibrated (per)fluorocarbon nanodroplets comprising an outer layer and an inner core, said outer layer comprising a biocompatible fluorinated surfactant and said inner core comprising a (per)fluorocarbon. The invention further relates to a method of preparation of said calibrated (per)fluorocarbon nanodroplets through microfluidic technique, and to their use for in vivo or in vitro diagnostic and/or for therapy.

First claim

1 ) A nanodroplet comprising an outer layer and an inner core, said outer layer comprising a biocompatible fluorinated surfactant and said inner core comprising a fluorocarbon, characterized in that the molar ratio between said biocompatible surfactant and said fluorocarbon is higher than 0.06, wherein said biocompatible fluorinated surfactant is selected from
(A) an amphiphilic dendrimer (Dendri-TAC) of generation n comprising:
a hydrophobic central core of valence 2 or 3;
generation chains attached to each respective open end of the central core and branching around the core; and
a hydrophilic terminal group at the end of each generation chain;
wherein n is an integer from 0 to 12 and identifies the hydrophilic terminal group comprising:
a mono-, oligo- or polysaccharide residue,
a cyclodextrin residue,
a peptide residue,
a tris(hydroxymethyl)aminomethane (Tris), or
a 2-amino-2-methylpropane-1,3-diol;
the hydrophobic central core is a group of formula (Ia) or (Ib)

wherein:
W is R F or a group selected from W 0 , W 1 , W 2 or W 3 :

R F is a C 4 -C 10 perfluoroalkyl or a C 1 -C 24 alkyl group,
R H is a C 1 -C 24 alkyl group,
p is 0, 1, 2, 3 or 4;
q is 0, 1, 2, 3 or 4;
L is a linear or branched C 1 -C 12 alkylene group, optionally interrupted by one or more —O—, —S—,
Z is C(═O)NH or NHC(═O),
R is a C 1 -C 6 alkyl group, and
e is at each occurrence independently selected from 0, 1, 2, 3 or 4,
(B) an amphiphilic linear oligomer (F-TAC) of formula II

wherein:
n is the number of repeating Tris units (n=DPn is the average degree of polymerization), wherein the term Tris indicates the tris(hydroxymethyl)aminomethane unit, and
i is the number of carbon atoms in the fluoroalkyl chain or a mixture thereof.

2 ) The nanodroplet according to claim 1 , wherein said amphiphilic dendrimer Dendri-TAC is selected from the group comprising the following compounds of formula IA

and of formula IB

3 ) The nanodroplet according to claim 1 , wherein said amphiphilic linear oligomer F-TAC is selected from the group comprising the following compounds of formula IIA

and of formula IIB

4 ) The nanodroplet according to claim 1 , wherein said fluorocarbon is a perfluorocarbon.

5 ) The nanodroplet according to claim 1 , wherein said molar ratio between said biocompatible fluorinated surfactant and said fluorocarbon is higher than 0.07.

6 ) An aqueous suspension comprising a nanodroplet according to claim 1 .

7 ) An aqueous suspension comprising a plurality of nanodroplets according to claim 1 , wherein said nanodroplets have a z-average diameter comprised between 100 nm and 1000 nm and a polydispersity lower than 0.25.

8 ) The aqueous suspension according to claim 6 further comprising trehalose.

9 ) A method for the preparation of an aqueous suspension of calibrated fluorocarbon nanodroplets, said method comprising the steps of:
a) Preparing an aqueous phase; b) Preparing an organic phase, wherein i) said aqueous phase comprises a biocompatible fluorinated surfactant selected from a Dendri-TAC, a F-TAC or a mixture thereof and the organic phase comprises a fluorocarbon or ii) said organic phase comprises a biocompatible fluorinated surfactant selected from a Dendri-TAC, a F-TAC or a mixture thereof and a fluorocarbon. c) Injecting said aqueous phase into a first inlet and said organic phase into a second inlet of a microfluidic cartridge, thereby mixing said aqueous phase and said organic phase in a mixing device of the microfluidic cartridge to obtain an aqueous suspension of calibrated fluorocarbon nanodroplets, and d) Collecting the aqueous suspension of calibrated fluorocarbon nanodroplets from the exit channel of the microfluidic cartridge.

10 ) The method according to claim 9 , wherein said aqueous phase comprises a biocompatible fluorinated surfactant selected from a Dendri-TAC, a F-TAC or a mixture thereof and said organic phase comprises a fluorocarbon.

11 ) The method according to claim 9 , wherein said fluorocarbon is a perfluorocarbon.

12 ) The method according to claim 11 , wherein said perfluorocarbon is selected from perfluoropentane, perfluorohexane, perfluorooctylbromide or a mixture thereof.

13 ) The method according to claim 9 , wherein the ratio between the volume of said aqueous phase and the volume of said organic phase is comprised between 1:1 to 5:1.

14 ) The method according to claim 9 , further comprising additional step e) wherein said collected suspension of calibrated fluorocarbon nanodroplets is diluted with an aqueous liquid.

15 ) The method according to claim 14 , wherein said aqueous liquid is water.

16 ) (canceled)

17 ) (canceled)

18 ) (canceled)

19 ) An aqueous suspension comprising a plurality of calibrated fluorocarbon nanodroplets obtainable by a method of preparation comprising the steps of:
a) Preparing an aqueous phase; b) Preparing an organic phase, wherein i) said aqueous phase comprises a biocompatible fluorinated surfactant, selected from Dendri-TAC, F-TAC or a mixture thereof, and the organic phase comprises a fluorocarbon or ii) said organic phase comprises a biocompatible fluorinated surfactant, selected from selected from Dendri-TAC, F-TAC or a mixture thereof and a fluorocarbon. c) Injecting said aqueous phase into a first inlet and said organic phase into a second inlet of a microfluidic cartridge, thereby mixing said aqueous phase and said organic phase in a mixing device of the microfluidic cartridge to obtain an aqueous suspension of calibrated fluorocarbon nanodroplets, and d) Collecting the aqueous suspension of calibrated fluorocarbon nanodroplets from the exit channel of the microfluidic cartridge, wherein said nanodroplets have a z-average diameter comprised between 100 nm and 1000 nm and a polydispersity lower than 0.25.

20 ) (canceled)

21 ) A method of diagnostic and/or therapeutic treatment comprising administering the aqueous suspension according to claim 6 to a patient.

Assignees

• Bracco Suisse Sa
• Avignon Univ

Inventors

• Melich Romain
• Bussat Philippe
• Cherkaoui Samir
• Contino-Pepin Christiane
• Desgranges Stéphane

Classifications

• A61K9/1075 Primary

  Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers (A61K9/0026 takes precedence) · CPC title

• A61K47/22

  Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones · CPC title

• A61K47/18

  Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids · CPC title

• A61K47/26

  Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin · CPC title

• A61K49/226 Primary

  Solutes, emulsions, suspensions, dispersions, semi-solid forms, e.g. hydrogels · CPC title