437
INDEXES How to find your way
The various subjects discussed i n the chapters are presented i n the Subject Indexes, as w e l l as the b o t a n i c a l names o f p l a n t s mentioned i n t h e t e x t . Solvent systems, d e t e c t i o n methods and various chromatographic techniques (ion-exchange,
reversed-phase,
ion-pair,
straight-phase) are n o t included i n the Subject Index. These subjects are d e a l t w i t h separately f o r each group o f a l k a l o i d s and may be found i n the l i s t o f contents o f each chapter.
A l l compounds w i t h a p e r t i n e n t reference t o r e t e n t i o n times o r d e t e c t i o n methods e i t h e r i n the t e x t , f i g u r e s o r tables are l i s t e d i n the compound index. F o r the various groups o f a l k a l o i d s , tables summarizing a l l the a v a i l a b l e l i t e r a t u r e are presented a t t h e end o f each chapter. Compounds l i s t e d i n these tables are n o t included i n the Compound Index. Hence t o f i n d a l l data r e l a t i n g t o a p a r t i c u l a r compound, i t may be necessary t o c o n s u l t both the Compound Index and the appropriate tables. SUBJECT INDEX GAS-L I QUID CHROMATOGRAPHY dcronychia a1 k a l o i d s
93-95
151, 152 d e r i v a t i z a t i o n 23, 151, 152 GC-MS 151
Amaryllidaceae a l k a l o i d s
Aporphine a l k a l o i d s
Caffeine analysis i n biological material
191- 194 a n a l y s i s i n food and beverages
114, 115, 128,
129, 147-150
190, 191 a n a l y s i s i n pharmaceutical
analysis i n biological material
128, 129, 148-150 d e r i v a t i z a t i on 23, 148-150 GC-MS
148, 150
GC-MS
53-56 dspidosperma a l k a l o i d s 166, 167
GC-MS
166
15-19, 40, 45, 46, 53, 81,
61-72 Cactus a l k a l o i d s 97-101 analysis i n b i o l o g i c a l m a t e r i a l 101 analysis i n p l a n t m a t e r i a l
97-101 Cactus a l k a l o i d s GC-MS
101
89, 90, 128, 136-138, 165, 166, 187, 189, 208 B-Carboline d e r i v a t i v e s 156, 157,
61-72
Belladonna a l k a l o i d s
derivatization
187, 192, 208
c a p i l l a r y gas chromatography
A r t e f a c t formation, see vol. 23A
Atropd a l k a l o i d s
194-198 187, 189, 208
preparations c a p i l l a r y GC
170 Cephalotaxus a l k a l o i d s
213-215
analysis i n plant material GC-MS 213
213, 214
Cinchona a l k a l o i d s 87-91 a n a l y s i s i n b i o l o g i c a l m a t e r i a l 87-89 analysis i n food and beverages 89 a n a l y s i s i n pharmaceutical prepara-
22, 101
t i o n s 87-90 c a p i l l a r y GC
89, 90
430
derivatization 22, 87-89, 91 GC-MS 89 Clavine alkaloids 176, 177 Cocaine metabolites 75-80 Coca leaves 73, 80, 8 1 Conium a1 kaloids 54 Datura a1 kaloids 61-72 Deactivation solid support 9-13 Derivatization of alkaloids f o r gas chromatography 21-24 Dihydroergotoxine alkaloids 177, 178, 180, 182
Drugs of abuse 113, 116, 127-136, 138- 14 1 analysis drug seizures 129-134,
142-144
173-176
Lupine alkaloids 55-59 Nicotine metabolites 42, 43, 45, 46, 47
Opium alkaloids 111-146 analysis i n biological material
analysis i n pharmaceutical preparations 125, 126 analysis in plant material 113, capillary GC 128, 136-138 derivatization 22, 23, 114-124, 126, 128, 129, 136, 137.
106-108
analysis in pharmaceutical preparations 105, 106 analysis in plant material 105 derivatization 22, 104 Ergot alkaloids 173-184 analysis in biological material 179
analysis in pharmaceutical perparations 176, 182, 183 derivatization 23, 24, 173-177 GC-MS 179. 180 Erythrina alkaloids 153, 154 derivatization 153, 154
142-144
GC-MS
116. 121-123, 127, 128
Papaveraceae a1 kaloids (see O p i u m alkaloids) 111-146 Physostigma a1 kaloids 166 Piperidine alkaloids 53, 54 analysis in plant material 53, 54
capillary GC 53 Piper nigrum alkaloids 53 Pseudotropine alkaloids 73-85 analysis in biological material 75-80
analysis in drug seizures 73,
153
Fused s i l i c a columns 15, 19, 81, 89, 90, 137. 138. 188
Glycoalkaloids 185, 186 Heteroyohimbine alkaloids
analysis i n opium 116-120, 125,
117
116, 134, 135
alkaloids 103-109 analysis in biological material
Ephedra
158, 159,
81
analysis in pharmaceutical preparations 74, 80 analysis in plant material 73, 80, 8 1
168-170 Hyoscyamus
154
LSO and derivatives
126
116, 127, 135, 136
capi 1 lary GC 136-138 derivatization 128-133, 135-137,
GC-MS
239-245)
Isoquinoline alkaloids 97-101, 111-
115, 116, 120-128, 136, 137
137
analysis in biological material
GC-MS
Imidazole alkaloids 217, 218 derivati zation 24 Indole alkaloids derivatization 23 Isolation from biological materials 388, 389 (see also vol. 23A 51-58,
alkaloids 61-72
capillary GC 8 1
439
derivatization GC-MS
21, 73-80, 83, 84
78-80
Pyridine alkaloids
33-52
42-47 35, 38-40, 41 34, 40-42
analysis i n plant material
21, 37, 43
35, 38-40,
45, 47 29-32
analysis i n plant material
c a p i l l a r y GC 31
21, 31, 32
Quinolizidine alkaloids
55-59
57, 58 159-162
160, 161
61-85 61-72
a n a l y s i s i n p h a n a c e u t i c a l preparations
analysis i n plant material
161
160
64-69
analysis i n plant material derivatization
Sample p r e p a r a t i o n
231, 388, 389
(see a l s o v o l . 23A 51-58, 239-245) Solanaceae a1 k a l o i d s ( s e e t r o p i n e 61-72
GC-MS
155-159, 175
uncaria a1 k a l o i d s
165-166
d e r i v a t i z a t i o n 24, 185, 186 61-72
Strychnos a1 k a l o i d s
162-165
168-170 165-166
analysis i n biological material
185, 186
Stramonium a l k a l o i d s
61-69
21, 65-69
67
Tryptamines
Vinca a l k a l o i d s
185, 186
Steroidal alkaloids
c a p i l l a r y GC
165, 166
derivatization GC-MS
analysis i n biological material 165
165
165
X a n t h i ne d e r i v a t i v e s
187-21 1
a n a l y s i s i n b i o l o g i c a l m a t e r i a1
a n a l y s i s i n pharmaceutical preparations
Tropane a l k a l o i d s Tropine a l k a l o i d s 67
analysis i n biological material
Solanurn a l k a l o i d s
21, 37, 43
45, 47
analysis i n biological material
Rauwolfia a1 k a l o i d s
alkaloids)
40, 45. 46
derivatization GC-MS
55-59
analysis i n plant material
GC-MS
34,
41
a n a l y s i s i n smoke 34, 40-42
P y r r o l i z i d i n e a1 k a l o i d s
GC-MS
42-47
40, 45, 46
derivatization
187. 208
Tobacco a l k a l o i d s analysis i n biological material
a n a l y s i s i n smoke derivatization
187, 189, 190,
202-208 GC-MS
34,
analysis i n plant material
c a p i l l a r y GC
189, 208
derivatization
analysis i n biological material
GC-MS
r a t i o n s 200 c a p i l l a r y GC
164
analysis i n plant material
162,
163 Symphytum a l k a l o i d s
190-194, 200-208 a n a l y s i s i n f o o d and beverages 190, 191 analysis i n phanaceutical pre-
31, 32
Theophyl 1i n e analysis i n biological material 190, 200-208 a n a l y s i s i n pharmaceutical prepa-
parations c a p i l l a r y GC derivatization
194-198, 200 187, 189, 208 24, 187, 189.
190, 199, 202-208 GC-MS
187, 192, 208
440
SUBJECT INDEX HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY Abbreviations f o r solvents
222
Aconite a l k a l o i d s 415, 416 A1 k y l ami nes 228 Aluminium oxide 229 Amaryllidaceae a l k a l o i d s 230, 287. 290,
291 A r t e f a c t formation (see v o l . 23A 53-56) Atropine and decomposition products
357-360,
362-368. 371 D i s s o l u t i o n s t a t i o n a r y phase 225.
228, 359 Diterpene a l k a l o i d s 415, 416 Drugs o f abuse 260-268, 297-330 analysis i n biological material
305, 308, 309, 324, 325 a n a l y s i s drug seizures 297, 300,
249-251. 254 Belladonna a l k a l o i d s 249-259 8 i sbenzyl isoquinol i n e a1 k a l o i d s 287,
288, 289, 292, 293 Cactus a l k a l o i d s 289, 290 Caffeine analysis i n b i o l o g i c a l f l u i d s
387-394, 399-401, 407-413 analysis i n food and beverages
389, 393, 394, 402, 414 metabolites 387-394, 399-401.
407-413 Catharanthus a l k a l o i d s
D i hydroergotoxine a1 k a l o i d s
332, 333,
347-349, 353 Chemically bonded s t a t i o n a r y phases c h a r a c t e r i z a t i o n 432-434 Chemisorption 225, 228 Cinchona a l k a l o i d s 269-285 analysis i n b i o l o g i c a l m a t e r i a l
269-273, 275-279, 283-285 analysis i n food and beverages
271. 272, 278, 285 analysis i n pharmaceutical preparat i o n s 272, 282, 283 C i r c u l a r dichroism detector 230, 290 Clavine a l k a l o i d s 360, 361. 367, 372 Cocaine metabolites 260, 265, 268 Colchicine and r e l a t e d a l k a l o i d s
417-419 Corrosion o f s t a i n l e s s s t e l l by mobile phase 226 Curare a l k a l o i d s 287, 288, 292 Detection methods 230, 231
301, 303, 304-310. 313-315, 326-328 Dynamic ion-exchange HPLC 227 Eburnane a l k a l o i d s 332, 334, 337-343, 347-353. 355. 356 Electrochemical d e t e c t i o n 230 E l l i p t i c i n e d e r i v a t i v e s 335, 336, 344 E l u o t r o p i c s e r i e s o f solvents f o r macroporous polymer r e s i n s 227 E l u o t r o p i c s e r i e s o f solvents f o r straight-phase chromatography (see v o l . 23A 5-7) E l u o t r o p i c s e r i e s o f solvents i n reversed-phase HPLC 224. 225 Ergometrine and decomposition products 357, 360 Ergot a l k a l o i d s 357-379 analysis i n biological material
357, 359, 362, 378-379 357, 358, 360, 361, 366. 368, 371-374
a n a l y s i s i n fungi
a n a l y s i s i n pharmaceutical preparations 357-360, 362, 366, 374-376 Ergotamine and decomposition products
357-359, 367 Ergotoxine a l k a l o i d s 357-361, 363-
368, 370-372 Fluorescence d e t e c t i o n 230 Free s i l a n o l groups i n s t a t i o n a r y phases 224 Glycoalkaloids 381-386
441
225, 229. 231
Guard columns
material
335, 354 Heroin metabolites 308 Harmane a l k a l o i d s
231, 273. 291, 366, 368, 372
rations
I d e n t i f i c a t i o n by using UV-absorption
322-324
HPLC-MS ratio
230. 237. 238. 302, 304
421-423 Indole a l k a l o i d s 331-379
287. 289. 290
P i l o c a r p i n e and decomposition products 421-423
Ion-exchange s t a t i o n a r y phases
432 I o n - p a i r HPLC 227, 228
P o l a r chemically bonded s t a t i o n a r y
characterization
phases
288. 290 I s o l a t i o n from b i o l o g i c a l material Ipecac a l k a l o i d s
388, 389 (see a l s o vol 51-58, 239-245)
. 23A
characterization
433. 434
Post-column d e r i v a t i z a t i o n 230,
249, 250-253,
290. 310, 360, 368 230, 251,
Pre-column d e r i v a t i z a t i o n
223. 287-330,
analysis i n biological material
288, 290, 296 a n a l y s i s i n pharmaceutical prepar a t i o n s 295, 296 a n a l y s i s i n p l a n t material
288.
290, 294, 295
252, 290 Pseudotropine a1 k a l o i d s
260-268
analysis i n b i o l o g i c a l m a t e r i a l
260, 265, 268 a n a l y s i s i n pharmaceutical prepar a t i o n s 264, 265
225, 226, 300
a n a l y s i s i n s t r e e t drugs Psilocybe a l k a l o i d s
analysis i n b i o l o g i c a l m a t e r i a l
357, 378, 379 a n a l y s i s i n drug seizures
357,
360, 366, 367, 371, 377, 378 Lumi-ergot a l k a l o i d s 360, 366 227, 235, 300, 316. 335, 354, 365, 426, 428
Macroporous polymer r e s i n s
Masking o f s i l a n o l groups
225, 226
331, 337, 343,
344, 347-349, 353, 355, 356 P y r i d i n e a l k a l o i d s 241-248 analysis i n b i o l o g i c a l m a t e r i a l 242, 246 analysis i n drugs of abuse analysis i n plant material
241-248
analysis i n plant material Quaternary alkylamines
Normal-phase s t a t i o n a r y phases
Quaternary amnonium compounds
434, 435
On-column preconcentration 231, 232,
359 223, 297-330
analysis i n biological material
303, 305, 308-310, 324, 325 analysis i n opium and p l a n t
245 243.
246 Pyrrolizidine alkaloids
297-330 Morphine metabolites 299. 305
Morphinan a l k a l o i d s
Opium a l k a l o i d s
260,
261. 266. 267
LSD and d e r i v a t i v e s
characterization
264
analysis i n plant material
Long chain a l k y l amines as m o d i f i e r i n solvents
(see opium
297-330
Phenylethylamines
HPLC 223
Isoquinoline alkaloids
305, 306, 310, 317,
Papaveraceae a l k a l o i d s alkaloids)
Imidazole a l k a l o i d s Ion-exchange
299, 300, 305, 306,
316, 317, 320, 321 a n a l y s i s i n pharmaceutical prepa-
241,
245 425, 428 250,
251, 254, 255, 287, 288, 290, 292, 336, 337. 425-432 Quinidine metabolites 269-273, 275-277, 279 Quinoline alkaloids
269-285
analysis i n biological material
269-273, 275-279, 283-285
44 2
analysis i n food and beverages 271, 272, 278, 285 analysis i n pharmaceutical preparations 272, 282, 283 Rauwolfia alkaloids 331. 335, 338, 341, 344 Reversed-phase HPLC 224-227 Reversed-phase ion-pai r HPLC 227, 228 Reversed-phase stationary phases characterization 432-433 Sample preparation 231, 388, 389, (see a l s o vol. 23A 51-58, 239-245) Senecio-a1 kaloids 241, 243, 244 S i l i c a gel 228, 229 S i l i c a gel pH 226, 229 S i l i c a gel stationary phases characterization 434, 435 Soap chromatography 227 Solanurn a1 kaloids 381-386 Solvent s e l e c t i v i t y (see vol. 23A 5-8) Stationary phases characterization 432-435 Steroidal a1 kaloids 381-386 Straight-phase HPLC 228 Straight-phase ion-pair HPLC 228 Strychnos a1 kaloids 331, 338, 341, 347-349, 355 Symphyturn-alkaloids 242, 244. 245 Tabernaemontana a1 kaloids 338 Terpenoid indole a1 kaloids 331-356 analysis i n biological material 332, 335, 337, 344, 351, 352, 354 analysis i n Pharmaceutical preparations 332, 337, 338, 343. 344, 350, 351, 354
analysis i n plant material 332, 335. 338, 343, 344, 347-349, 353, 355, 356 Theophyl l i n e analysis i n biological materials 387-394, 399-401, 407-413 metabolites 387-394, 399-401, 407413 Tobacco alkaloids 241-248 analysis i n biological material 242, 246 analysis i n drugs of abuse 245 analysis i n plant material 243, 246 Trace enrichment 231, 232, 359 Tropane alkaloids 249-268 Tropine alkaloids 249-259 analysis i n biological material analysis i n pharmaceutical preparations 249-252, 254. 255, 257259 analysis i n plant material Uric acid derivatives 387, 390, 391, 399-401 veratrurn alkaloids 383 Vinca alkaloids 332, 334, 337-343, 347-353, 355, 356 Xanthine alkaloids 387-414 analysis i n biological materials 387-394, 399-401, 407-413 analysis i n food and beverages 389, 393, 394, 402, 414 analysis i n pharmaceutical preparations 389, 393, 394, 401, 404407