The aim of this study was to investigate the potential cytotoxicity of solid lipid nanoparticles (SLN) loaded with sildenafil. The SLNs were tested as a new drug delivery system (DDS) for the inhalable treatment of pulmonary hypertension in human lungs. Solubility of sildenafil in SLN lipid matrix (30:70 phospholipid:triglyceride) was determined to 1% sildenafil base and 0.1% sildenafil citrate, respectively. Sildenafil-loaded SLN with particle size of approximately 180 nm and monomodal particle size distribution were successfully manufactured using a novel microchannel homogenization method and were stable up to three months. Sildenafil-loaded SLN were then used in in vitro and ex vivo models representing lung and heart tissue. For in vitro models, human alveolar epithelial cell line (A459) and mouse heart endothelium cell line (MHEC5-T) were used. For ex vivo models, rat precision cut lung slices (PCLS) and rat heart slices (PCHS) were used. All the models were treated with plain SLN and sildenafil-loaded SLN in a concentration range of 0-5000 µg/ml of lipid matrix. The toxicity was evaluated in vitro and ex vivo by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Median lethal dose 50% (LD50) values for A549 cells and PCLS were found to be in the range of 1200-1900 µg/ml while for MHEC5-T cells and precision cut heart slices values were found between 1500 and 2800 µg/ml. PCHS showed slightly higher LD50 values in comparison to PCLS. Considering the toxicological aspects, sildenafil-loaded SLN could have potential in the treatment of pulmonary hypertension via inhalation route.
Experimental investigations of the effect of microchannel geometry on high-pressure dispersion and emulsification were carried out. Customized microchannels of varying geometric principles were fabricated in silicon and steel. In order to characterize the process efficiency of microchannel geometries, the effects of the process parameters (mean velocity, Reynolds number, and local pressure drop) were examined and correlated to the dispersion and emulsification results. It is demonstrated that high pressure losses focused at a small channel length and high velocity gradients lead to high stress intensities and, in consequence, to low particle or droplet sizes. Thus, 2D orifices were successfully further improved regarding their process efficiency by adding a third-dimension constriction.
In the development of colloidal lipid drug delivery systems (DDS), the localization of the drug within the DDS, the protective potential of the DDS as well as the compatibility of the drug with the excipients are of special interest. In this study, Coumarin 6 (C6), a fluorescent dye frequently used to facilitate the traceability of DDS in vitro, is demonstrated as a tool to gain insight into the aforementioned properties by fluorescence spectroscopy. Both ways of loading C6 to solid colloidal DDS (pre‐loading to the lipid matrix or post‐loading to the ready DDS after its processing) led to a localization of C6 in the interfacial layer between solid lipid nanoparticles (SLN) and aqueous medium. In the case of pre‐loading, C6 is homogenously distributed in emulsion droplets and expelled from the lipid matrix due to crystallization. Nanoemulsions distributed C6 in the liquid lipid matrix itself and cause a hypsochromic shift of fluorescence spectra. Larger surface areas of emulsion droplets due to smaller droplet sizes displayed more interaction of C6 with the aqueous phase as a bathochromic shoulder in fluorescence spectra. Measured fluorescence intensity was linearly dependent on light scattering of colloidal DDS of the same excipients. A simple method to evaluate the protective properties of DDS was presented and displayed that (i) nanoemulsions provide more protection compared with SLN and (ii) higher phospholipid concentration improve the protection within SLN.
Practical applications: In the development of colloidal DDS, it is important to identify the localization and distribution of a (model) drug in compartments within the disperse system. The simple approach by fluorescence spectroscopy presented in this study supplies information about the localization of drug substances with properties comparable with the fluorescent probe used. The results assist formulation development as a quick screening tool to elucidate (i) the localization of the probe, (ii) the microenvironment of the probe (e.g., differentiation of the physical state of the disperse phase), and (iii) the protection of the probe against damaging agents from the aqueous phase.
The fluorescent dye Coumarin 6 was applied as model drug in colloidal lipid drug delivery systems. Fluorescence spectroscopy proved able to identify the localization of the model compound, the physical state of the dispersed phase, and the protective potential of the DDS, especially dependent on phospholipid concentration.
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