Wound healing activity of curcumin conjugated to hyaluronic acid: in vitro and in vivo evaluation.

Curcumin is a promising wound healing agent but its clinical application is limited due to hydrophobicity and lack of stability. In this article, we report the results of a study on wound healing efficacy of curcumin conjugated to hyaluronic acid (HA) which is a natural polysaccharide known to influence the healing process. Studies on proliferation, antioxidant activity and scratch wound healing carried out in human keratinocyte cells revealed that HA-conjugated curcumin treatment enhanced cell proliferation, decreased oxidative damage induced by H2O2 and also improved migration of cells in scratch wounds as compared to treatment with native curcumin. HA conjugated curcumin exhibited bactericidal activity in dark and phototoxicity when irradiated with blue light against antibiotic resistant bacteria. Furthermore, wound healing efficacy studied in diabetic mice demonstrated that topical application of the conjugate on wounds led to better healing as compared to treatment with HA-free curcumin and HA alone. These results suggest that HA conjugation is a promising formulation of curcumin for enhancing its healing efficacy.

Evaluation of digital infra-red thermal imaging as an adjunctive screening method for breast carcinoma: a pilot study.

BACKGROUND: Early screening plays a pivotal role in management of breast cancer. Given the socio-economic situation in India, there is a strong felt need for a screening tool which reaches the masses rather than waiting for the masses to reach tertiary centers to be screened. Digital infra-red thermal imaging (DITI) or breast thermography as a screening test offers this possibility and needs to be carefully assessed in Indian scenario. METHODS: The study involved 1008 female patients of age 20-60 years that had not been diagnosed of cancer of breast earlier. All the subjects in this population were screened for both the breasts using DITI. Based on the measured temperature gradients (ΔT) in thermograms, the subjects were classified in one of the three groups, normal (ΔT ≤ 2.5), abnormal (ΔT > 2.5, <3) and potentially having breast cancer (ΔT ≥ 3). All those having (ΔT > 2.5) underwent triple assessment that consisted of clinical examination, radiological and histopathological examination. Those with normal thermograms were subjected to only clinical examination. RESULTS: Forty nine female breasts had thermograms with temperature gradients exceeding 2.5 and were subjected to triple assessment. Forty one of these which had ΔT ≥ 3 were proven to be having cancer of breast and were offered suitable treatment. Eight thermograms had temperature gradients exceeding 2.5 but less than 3. Most of these were lactating mothers or had fibrocystic breast diseases. As a screening modality, DITI showed sensitivity of 97.6%, specificity of 99.17%, positive predictive value 83.67% and negative predictive value 99.89%. CONCLUSION: Based on the results of this study involving 1008 subjects for screening of breast cancer, thermography turns out to be a very useful tool for screening. Because it is non-contact, pain-free, radiation free and comparatively portable it can be used in as a proactive technique for detection of breast carcinoma.

Photodynamic action of Rose Bengal silica nanoparticle complex on breast and oral cancer cell lines.

Rose Bengal, an anionic photosensitizer was conjugated to organically modified silica nanoparticles having 3-amino propyl groups by electrostatic or covalent interaction. The drug-nanoparticle complexes were characterized by FTIR, light scattering and zeta potential measurements. Significant changes were observed in the spectroscopic properties of the drug when it is conjugated with nanoparticles. The toxicity of the free drug and drug-nanoparticle complex was studied against oral (4451) and breast (MCF-7) cancer cell lines. Both complexes with nanoparticles were more phototoxic than free Rose Bengal, with the covalent complex being the more effective. Studies carried out on cellular uptake, photostability and singlet oxygen generation suggest that enhanced phototoxicity is primarily due to the enhanced uptake of the drug-nanoparticle complex.

NIR femtosecond laser induced hyper-Rayleigh scattering and luminescence from silver nanoprisms.

The nonlinear response of silver nanoprisms (edge length 40 +/- 5 nm and thickness 4.5 +/- 0.5 nm) was studied by exciting with NIR femtosecond pulses (780-880 nm). These nanostructures were observed to generate hyper-Rayleigh scattering (HRS) and broadband luminescence. While HRS showed the expected second order power dependence, the luminescence was observed to follow a third order excitation power dependence. Both HRS and luminescence were observed to be dipolar in nature. The first hyperpolarizability of the nanoprisms was found to be an order of magnitude higher than approximately 15 nm sized nanospheres.

Spectroscopic investigations on the binding of the photosensitizer Chlorin p6 with amine-modified silica nanoparticles in aqueous media.

Absorption and emission properties of the amphiphilic photosensitizer Chlorin p6 were investigated in aqueous medium in the presence of silica nanoparticles (SiNPs) having positively charged amino groups. The results of these studies reveal that the acid-base ionization equilibrium of Chlorin p6 in aqueous medium is significantly affected as a result of strong electrostatic binding between the negatively charged drug and SiNP. The spectroscopic signature of the drug bound to SiNPs suggests that the tri-anionic form of the drug remains bound to the positively charged SiNPs at pH 8.0. As the pH is progressively decreased the formation of hydrophobic aggregates is disrupted significantly due to the presence of electrostatic binding force, which competes with intermolecular hydrophobic forces. The interplay of hydrophobic and electrostatic forces in the drug-nanoparticle binding process might affect the relative uptake and photodynamic efficacy of the free drug and the drug-nanoparticle complex in cancer cells.

Nile Blue in Triton-X 100/benzene-hexane reverse micelles: a fluorescence spectroscopic study.

We report the observation of ground state prototropic equilibrium of the dye Nile Blue in Triton-X 100/benzene-hexane reverse micellar system. In the absence of water, the deprotonated form of the dye is predominant. Addition of water produces the protonated form. At highest water loading, the equilibrium is still shifted towards the deprotonated form as revealed by the absorption spectrum. In neat Triton-X 100 also, the dye is present almost predominantly in the deprotonated form as revealed by the absorption spectrum. The average fluorescence lifetime of the dye is greater in neat Triton-X 100 than in Triton-X 100 reverse micelles, when no water is added. Addition of water to the reverse micelles increases the average lifetime of the deprotonated species. We offer possible explanations to the above observations by discussing the structure and properties of the Triton-X 100/benzene-hexane reverse micelles.

The effect of pH and surfactant on the aggregation behavior of chlorin p6: a fluorescence spectroscopic study.

Steady state and time-resolved fluorescence properties of chlorin P6, a potential drug for photodynamic therapy, have been investigated as functions of pH. A decrease in pH of the medium has been shown to cause protonation of the ionizable carboxylic acid side chain, leading to an increase in hydrophobicity and consequent aggregation. The aggregates dissociate on further protonation. The dissociation is explained in terms of formation of cations and their mutual repulsion. A synchronous fluorescence spectroscopic study revealed the presence of two anionic forms in equilibrium at physiological pH, with a shift in the equilibrium on slight decrease in the pH. The anionic nature of chlorin P6 in aqueous solutions at physiological pH has been confirmed by complexation with surfactants. The nature of the charge on the headgroups of the surfactants has been found to govern the formation of chlorin-surfactant complexes.