Reflectance analogue

The analogue system simply corrects for the non-linearity of the source and detector. The reflectance analogue system, given as 7.8.29. on the next page. 

A 2-h incubation with another PGE2 analogue, nocloprost (9P-chloro-DMPG) protects normal human fibroblasts but has no effect on the survival of colon adenocarcinoma cells exposed to 10 Gy (1000 rad) (218). Nocloprost protects against radiation-induced DSBs in normal cells but not in tumor cells. Moreover, incubation using nocloprost for 2 h after irradiation enhances the rate of DSB rejoining in fibroblasts but not in adenocarcinoma cells. These data possibly reflect a different distribution of PG receptors on the plasma membrane of the two cell types. 

An important issue in the thermodynamics of confined fluids concerns their symmetry which is lower than that of a corresponding homogeneous bulk phase because of the presence of the substrate and its inherent atomic structure [52]. The substrate may also be nonplanar (see Sec. IV C) or may consist of more than one chemical species so that it is heterogeneous on a nanoscopic length scale (see Sec. VB 3). The reduced symmetry of the confined phase led us to replace the usual compressional-work term —Pbuik F in the bulk analogue of Eq. (2) by individual stresses and strains. The appearance of shear contributions also reflects the reduced symmetry of confined phases. 

The steric crowding introduced in the latter by the four ethyl substituents inhibits nucleophilic attack at platinum, so that complexes of this type tend to undergo substitution by a dissociative mechanism [89]. The complex of the more rigid ligand, 2,2, 2"-terpyridyl, Pt(terpy)Cl+, is found to be about 103 to 104 times more reactive to substitution than the dien analogue this is ascribed to steric strain [90], which is reflected in the short Pt—N bond to the central nitrogen (Pt-N some 0.03 A shorter than the other two Pt-N bonds) and N—Pt—N bond angles of 80-82°). 

LEED is the surface analogue of X-ray diffraction. As the name indicates, the major difference is that one uses electrons instead of X-rays. As electrons of low kinetic energy (40-200 eV) do not penetrate very far into the material without losing energy, the elastically reflected electrons carry only information on the outermost layers of the surface (see Eig. 4.7). 

The requirements for an instrumental method of specifying reflected color include a light source, the colored object and a detector. What this means is that all we need is a source, an object and a detector. However, since the response characteristics of these optical components are not linear, nor flat, we need an analogue system in order to be able to measure color. 

However, these analogues are actually hypothetical. The reason for this is that it is nearly impossible to obtain optical measurement components, such as the source and the detector, whose response to light across the visible spectrum is flat (or nearly so). However, this is not an impossible task and we find that an excellent match can be obtained to the transmission functions of 7.8.21., i.e.-those of the Standard Observer. This is typical for commercially available instruments. Now, we have an instrument, called a Colorimeter, capable of measuring reflective color. 

Tables 6.8-6.11 illustrate the wide range of C3 side-chain modified A -THC analogues that have been reported in the literature, together with associated in vitro and in vivo data. The affinity of classical cannabinoid analogues for the CBi receptor has been shown to correlate with depression of spontaneous activity and the production of antinociception, hypothermia and catalepsy in mice, and with psychomimetic activity in humans [93]. However, in some cases, there were unexplained differences between the observed trends in binding affinity and the trends in activity in mouse behavioural models. This may point to differences in efficacy among full agonists, partial agonists and antagonists/inverse agonists, or may reflect differences in in vivo metabolism or blood-brain barrier penetration or a combination of these factors.

Table 6.1 summarizes the thermodynamic parameters relating to the macrocyclic effect for the high-spin Ni(n) complexes of four tetraaza-macrocyclic ligands and their open-chain analogues (the open-chain derivative which yields the most stable nickel complex was used in each case) (Micheloni, Paoletti Sabatini, 1983). Clearly, the enthalpy and entropy terms make substantially different contributions to complex stability along the series. Thus, the small macrocyclic effect which occurs for the first complex results from a favourable entropy term which overrides an unfavourable enthalpy term. Similar trends are apparent for the next two systems but, for these, entropy terms are larger and a more pronounced macrocyclic effect is evident. For the fourth (cyclam) system, the considerable macrocyclic effect is a reflection of both a favourable entropy term and a favourable enthalpy term. 

---