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Here we additionally introduce a Flash NanoPrecipitation technique that has been adopted for encapsulating biologics in nanoparticles (40-200 nm) at high loadings (50-seventy five wt.%) and high encapsulation efficiencies. The required nonapeptide acids were prepared by the stable section method on chloromethyl-polystyrene resin using HF/anisole deprotection. The compounds have been prepared by coupling of the corresponding nona-peptide acids with semicarbazide hydrochloride by the N,N′-dicyclohexylcarbodiimide/1-hydroxybenzotriazole procedure. The effect of combination of the hydrophilic aza-Gly substitution (NHNHCO) at place 10 with hydrophobic, unnatural D-amino acids in position 6 on the potency of luteinizing hormone-releasing hormone (LH-RH) analogues has been investigated. Previously the aza-Gly residue was shown to provide protection from enzymatic cleavage and result in potency will increase in a less hydrophobic collection. Furthermore, evidence that the proper disulphide bonds (Cys53Cys165; Cys182Cys189) have been formed in rhGH throughout secretion has been shown by a mixture of tryptic fingerprint and amino acid analysis. Proteins are valued based on their important amino acid composition
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