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The effect of a pulsing electromagnetic field (PEMF) on bone ingrowth into porous hydroxyapatite (HA) and porous tricalcium phosphate (TCP) implanted in rabbit tibiae was studied. To quantitate the biological response, a recently developed method of surface measurement using a scanning electron microscope was used. The morphometrical findings in the HA pores demonstrated a significantly greater amount of bone and thicker bone trabeculae in the PEMF group as compared with the nonpulsed control group at 3 to 4 weeks postimplantation. No significant differences for these parameters were found in the TCP pores. Histologically, more bone and wider bone trabeculae were observed in the HA implants for the PEMF-treated animals at the early time periods when compared with those of the control animals. Alternatively, the histological findings of the TCP implants were similar between these two groups. These histological results tended to correlate with the morphometrical data. Together, these results suggest that accelerated bone formation and bone maturation occurred in response to PEMF in the HA pores but was without effect in the TCP pores. This stimulatory effect is most significant after 3-4 weeks of PEMF stimulation.

In order to clarify the dose/response characteristics of continuous passive motion (CPM), the repair response of full thickness articular cartilage defects was studied in a rabbit model. The following combinations of CPM and immobilization (Imm) were utilized: CPM, 24 h/day; CPM, 8 h/day and Imm, 16 h/day; CPM, 2 h/day and Imm 22 h/day; Imm 24 h/day; and normal cage activity. These regimens were used only in the initial week and then all rabbits were permitted to move freely in their cages, except for a sixth Imm-CPM group that was kept immobilized in the initial week and then CPM 24 h/day for another week. The CPM 24 h/day and the CPM 8 h/day groups (groups 1 and 4, respectively) showed better repair than the other groups, i.e., better surface congruity, larger positive Safranin-O staining area, and greater number of chondrocytes in the repair tissue. The CPM 2 h/day group (group 3), however, showed only slightly better repair than the Imm group (group 4). The CPM following immobilization was not effective to overcome the harmful effect of immobilization. We conclude that in the present model, CPM for 8 or 24 h/day is effective for adequate cartilage repair even with some component of immobilization. Its application should be at least 8 h/day. On the contrary, if CPM is delayed for a week following immobilization, the effect of CPM on cartilage will be reduced.

Three nitrile oxides (MeOCOC≡N→O, PhC≡N→O, and EtC≡N→O) were effectively generated in situ by dehydration of the corresponding primary nitro compounds (RCH2NO2) with PhSO2Cl or ClCOOEt in the presence of triethylamine. Various cycloadducts were prepared by the reaction of them with dipolarophiles. Some advantages of these methods are described in comparison with other known methods.

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