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Research Article

Development, characterization and toxicological evaluations of phospholipids complexes of curcumin for effective drug delivery in cancer chemotherapy

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Pages 1057-1068 | Received 11 Mar 2014, Accepted 17 Jun 2014, Published online: 17 Jul 2014

Figures & data

Table 1. Inter and intra assay variations of CU.

Table 2. Solubility of CU, PC, HSPC, CU–PC-C, CU–HSPC-C and physical mixture in water and n-octanol at 25 °C.

Figure 1. FT-IR of CU, CU–PC-C and CU–HSPC-C.

Figure 1. FT-IR of CU, CU–PC-C and CU–HSPC-C.

Figure 2. SEM of CU-PC-C (A) and CU-HSPC-C complex (B).

Figure 2. SEM of CU-PC-C (A) and CU-HSPC-C complex (B).

Figure 3. In vitro release study of plain CU, CU-PC-C and CU-HSPC-C at different time points. Values are mean ± SEM (n = 3).

Figure 3. In vitro release study of plain CU, CU-PC-C and CU-HSPC-C at different time points. Values are mean ± SEM (n = 3).

Figure 4. In-vitro hemolysis study of CU, CU-PC-C and CU-HSPC-C.

Figure 4. In-vitro hemolysis study of CU, CU-PC-C and CU-HSPC-C.

Figure 5. In-vitro cytotoxicity of CU, CU-PC-C and CU-HSPC-C on MCF-7 cell.

Figure 5. In-vitro cytotoxicity of CU, CU-PC-C and CU-HSPC-C on MCF-7 cell.

Figure 6. Hematological parameters of different groups in Wister rats.

Figure 6. Hematological parameters of different groups in Wister rats.

Figure 7. Biochemical parameters of different groups in Wister rats.

Figure 7. Biochemical parameters of different groups in Wister rats.

Figure 8. Representative photomicrographs of (A) liver (Group I), (B) liver (Group III), (C) kidney(Group I), (D) kidney (Group III), (E) intestine (Group I), (F) intestine (Group III), (G) spleen (Group I), (H) spleen (Group III), [Cv: central vein; Lf: lymphoid follicle; Gm: glomerulus; Tb: tubule; M: mucosa; and Sm: sub-mucosa]. The various organ sections were stained with hematoxylin and eosin (10×).

Figure 8. Representative photomicrographs of (A) liver (Group I), (B) liver (Group III), (C) kidney(Group I), (D) kidney (Group III), (E) intestine (Group I), (F) intestine (Group III), (G) spleen (Group I), (H) spleen (Group III), [Cv: central vein; Lf: lymphoid follicle; Gm: glomerulus; Tb: tubule; M: mucosa; and Sm: sub-mucosa]. The various organ sections were stained with hematoxylin and eosin (10×).

Figure 9. (A and B) Results of the micronucleus assay conducted in bone marrow cells of mice. ***p < 0.0001.

Figure 9. (A and B) Results of the micronucleus assay conducted in bone marrow cells of mice. ***p < 0.0001.

Figure 10. Results of the chromosome aberration assay conducted in bone marrow cells of mice. ***p < 0.0001.

Figure 10. Results of the chromosome aberration assay conducted in bone marrow cells of mice. ***p < 0.0001.

Figure 11. Representative bone marrow cells stained with May Grunwald–Giemsa and exhibiting the presence of micronuclei [micronucleated normochromatic erythrocyte (MNPCE)].

Figure 11. Representative bone marrow cells stained with May Grunwald–Giemsa and exhibiting the presence of micronuclei [micronucleated normochromatic erythrocyte (MNPCE)].

Figure 12. (A) Normal chromosomes in mice bone marrow cells. (B) Types of chromosomal aberrations in bone marrow cells of mice treated with cyclophosphamide.

Figure 12. (A) Normal chromosomes in mice bone marrow cells. (B) Types of chromosomal aberrations in bone marrow cells of mice treated with cyclophosphamide.
Supplemental material

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