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. 2022 Sep 21;14(10):2003. doi: 10.3390/pharmaceutics14102003

Table 5.

Overview of solubility enhancement reported for co-crystal drugs.

# Solubility Evaluation (UV, HPLC) Sample Folds Ref.
3C In vitro Ciprofloxacin-thymol (1:2) 4 [118]
5C UV Brexpiprazol-catechol (1:1) 2.5 [120]
Brexpiprazol-succinic acid (1:1) 2.5
6C UV Quercetin-malonic acid (1:2) 1.056 [121]
7C UV Paracetamol-trimethylglycine * (1:1) 0.82 [44]
11C UV Ciprofloxacin-nicotinic acid (1:1) 20 (in water) [124]
1.5
Ciprofloxacin-isonicotinic acid (1:1) 20
2.5
13C HPLC Acetazolamide-4-aminobenzoic acid * (1:1) 2.5 [67]
2.17
15C IDR β-lapachone-resorcinol (1:1) 2 [127]
16C UV Norfloxacin-nicotinic acid (with EtOH) pH = 3 No change [128]
Norfloxacin-nicotinic acid (with EtOH) pH = 6.1 2
Norfloxacin-nicotinic acid (with EtOH) pH = 8.5 <2
17C UV (Powder dissolution) Chlorothiazide-DL-proline (w/acetonitrile-water) 1.05 [129]
Chlorothiazide-L-proline hydrate (w/acetonitrile-water) Lower value than the initial drug
Chlorothiazide-D-proline hydrate (w/acetonitrile-water)
19C HPLC (In vitro release test) Ferulic acid-nicotinamide 2.4 [131]
Ferulic acid-isonicotinamide 3.1
Ferulic acid-urea 1.1
21C HPLC Itraconazole-4-hydroxybenzamide form II (1:2) 225 [133]
Itraconazole-4-aminobenzoic acid (1:1) 64