Methoxy-poly(ethylene glycol)s bearing a terminal cholanic moiety (mPEG5kDa-cholane, mPEG10kDa-cholane and mPEG20kDa-cholane) were physically combined with recombinant human growth hormone (rh-GH) to obtain supramolecular assemblies for sustained hormone delivery. The association constants (Ka) calculated by Scatchard analysis of size exclusion chromatography (SEC) data were in the order of 10(5)M(-1). The complete rh-GH association with mPEG5kDa-cholane, mPEG10kDa-cholane and mPEG20kDa-cholane was achieved with 7.5±1.1, 3.9±0.4 and 2.6±0.4 w/w% rh-GH/mPEG-cholane, respectively. Isothermal titration calorimetry (ITC) yielded association constants similar to that calculated by SEC and showed that rh-GH has 21-25 binding sites for mPEG-cholane, regardless the polymer molecular weight. Dialysis studies showed that the mPEG-cholane association strongly delays the protein release; 80-90% of the associated rh-GH was released in 200h. However, during the first 8h the protein formulations obtained with mPEG10kDa-cholane and mPEG20kDa-cholane showed a burst release of 8 and 28%, respectively. Circular dichroism (CD) analyses showed that the mPEG5kDa-cholane association does not alter the secondary structure of the protein. Furthermore, mPEG5kDa-cholane was found to enhance both the enzymatic and physical stability of rh-GH. In vivo pharmacokinetic and pharmacodynamic studies were performed by subcutaneous administration of rh-GH and rh-GH/mPEG5kDa-cholane to normal and hypophysectomised rats. The study showed that mPEG5kDa-cholane decreases the maximal concentration in the blood but prolongs the body exposure of the protein, which resulted in 55% bioavailability increase. Finally, rh-GH formulated with mPEG5kDa-cholane yielded prolonged weight increase of hypophysectomised rats as compared to rh-GH in buffer or formulated with mPEG5kDa-OH. After the second administration the weight of the animals treated with rh-GH formulated with mPEG5kDa-cholane was about 2 times higher than that obtained with equal dose of non-formulated rh-GH.
A novel soluble supramolecular system for sustained rh-GH delivery
SALMASO, STEFANO;BERSANI, SARA;SCOMPARIN, ANNA;BALASSO, ANNA;BRAZZALE, CHIARA;BARATTIN, MICHELA;CALICETI, PAOLO
2014
Abstract
Methoxy-poly(ethylene glycol)s bearing a terminal cholanic moiety (mPEG5kDa-cholane, mPEG10kDa-cholane and mPEG20kDa-cholane) were physically combined with recombinant human growth hormone (rh-GH) to obtain supramolecular assemblies for sustained hormone delivery. The association constants (Ka) calculated by Scatchard analysis of size exclusion chromatography (SEC) data were in the order of 10(5)M(-1). The complete rh-GH association with mPEG5kDa-cholane, mPEG10kDa-cholane and mPEG20kDa-cholane was achieved with 7.5±1.1, 3.9±0.4 and 2.6±0.4 w/w% rh-GH/mPEG-cholane, respectively. Isothermal titration calorimetry (ITC) yielded association constants similar to that calculated by SEC and showed that rh-GH has 21-25 binding sites for mPEG-cholane, regardless the polymer molecular weight. Dialysis studies showed that the mPEG-cholane association strongly delays the protein release; 80-90% of the associated rh-GH was released in 200h. However, during the first 8h the protein formulations obtained with mPEG10kDa-cholane and mPEG20kDa-cholane showed a burst release of 8 and 28%, respectively. Circular dichroism (CD) analyses showed that the mPEG5kDa-cholane association does not alter the secondary structure of the protein. Furthermore, mPEG5kDa-cholane was found to enhance both the enzymatic and physical stability of rh-GH. In vivo pharmacokinetic and pharmacodynamic studies were performed by subcutaneous administration of rh-GH and rh-GH/mPEG5kDa-cholane to normal and hypophysectomised rats. The study showed that mPEG5kDa-cholane decreases the maximal concentration in the blood but prolongs the body exposure of the protein, which resulted in 55% bioavailability increase. Finally, rh-GH formulated with mPEG5kDa-cholane yielded prolonged weight increase of hypophysectomised rats as compared to rh-GH in buffer or formulated with mPEG5kDa-OH. After the second administration the weight of the animals treated with rh-GH formulated with mPEG5kDa-cholane was about 2 times higher than that obtained with equal dose of non-formulated rh-GH.
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