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Biopharmaca Research

Center

Bogor

Agricultural University

frET)

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Drs. (eflufr

I,li[o[o,

Apt.

As

Poslel Presenler

In

The

Inlernolionol

Symposium

on

Biomedicines

wtlhlherc

'

Biodtversily

on

Trodilionol

Biomedicines

for

H u

mo

n

H

eolth

ondWelfore'

I

,l

r*l

.

fr

ti

It

(2)

-98350-0-

3

ffi

ilAmf{A

ON

BIOMED

Biopharmaca

Research

Center

Bogor

Agricultural

UniversitY

Bogor

-

Indonesia

Po$ltJM

l8'n

and

19'n

September

2003

Theme:

(3)

PROCEEDINGS

INTERNATIONAL

SYMPOSIU

M

ON

BIOMEDICINES

Bogor,

18th

-

19th

September

2003

Editor:

Dr. Yulin Lestari

Prof.

Dr. Latifah

I(

Darusman. MS

Drs.

Edy

Djauhari, MSi

Drh.

Sulistiyani,

PhD

Dr.

Nampiah

I

Sukarno

Irmenida Batubara'

SSi'

MSi

Drh.

Sriwijayani

BIOFARMACA

RESEARCH

CENTER

BOGOR

AGRICULTURAL UNIVERSITY

(4)

PROCEEDINGS

INTERNATIONAL

SYMPOSIU

M

ON

BIOMEDICINES

Bogor,

18th

-

19th

September

2A03

B

iodiversity'on Traditional

Biomedicines

for

Human

Health

and

Welfare

Organized

by:

Biopharmaca

Research

Center

Bogor

Agricultural

UniversitY

Intemational Symposium on Biomedicines (2203: Bogor)

Proceedings Intemational Symposium on Biomedicines:

Bogor,

18 September 2003:

Biodiversity

on Traditional Biomedicines

for

Human Health and

Welfare.

-

Bogor: Pusat Studi Biofarmaka LPPM IPB, 2004

364

hlm.;

29 cm

ISBN

: 979-98350-0-3

(5)

PROCEEDINGS OF

INTERNATIONAL SYMPOSIUM ON BIOMEDICINES

Quality Control

of

Physicochemistry

Parameter

of

Oil

and Eugenol Isolated

from

Flos and Leaves of Eugenia

caryphyllala

Thunb

inToli-toli'

Central

if

Sulawesi

Endang D., Sadria,

R llahyuningtas,

C

Anwar

The

Formulation

of

Granules

Effervescent Tea Teguh

ll/idodo, Lucia Hendriati,

Arief

ll/ijayanto

Inventory

and

Conservation

of

Medicinal

Plants

N.

Bermawie, S, Fatimah Syahid,

N Novo Kristina

34t

346

349

(6)

PROCEEDINGS OF

INTERNATIONAL SYMPOSIUM ON BIOMEDICINES

The

Formulation

of

Granules Effervescent

Tea

Teguh

llidodo,

Lucia Hendriati,

Arief llijayanto

Faculty of Pharmacy, Widya Mandala Surabaya Catholic University

Abstract

Tea as beverage

is

one

of

the

most popular

drinks

and has many advantages

for

health. Granule effervescent is popular dosage

form

since its unique and interesting

from.

This

research

is

try

to

formulate the tea

into

the granule effervescent which

will

become an altemative to serve tea easier and more interesting. The capability

of

granules

to flow

at production, pouring process, and bubbles release when granule dissolves are influenced

by distribution

of

granule size and dissolved

time. In

this research,

four

granule effervescent formula

with

variety

of

PVP

K-30

concentration as a binder are made. The granule product are evaluated on

its

flowability,

angle

of

repose,

moisture

content, granule

size distribution and

dissolved

time.The

result

show

that

the variety

of

PVP K-30

concentration has

a

different

result

on

its

flowability,

angle

of

repose, moisture content granule size distribution and dissolved time. Between the formulas, formula

with

0,5% PVP

K-3

0 has a better result.

Key word : tea, effervescent, granule

Introduction

Leaves

oftea

are known since

many

centuries

have

advantage

for

health.

It

makes tea become one

ofthe

most popular non alcoholic

drinks.

The

constituens

in

tea

leaves

are

tannin, coffein.

theophyllin, theobromin, several vitamines, sugar,

pectin

and

selulosa.

(Adisewojo,

1982). Some

advantages

of

tea

are

analeptic, heart

and brain

stimulant antioksidant. degenerative prcventives,

antiviral,

antifungal

and

antibacterial

agent

(Astuti,

2001 ,

Hamdan

&

Jonosewojo, 2001 ).

The

increasing

in

tea

consumption

needs

an

inovatif

ploduel

to

nrakc

an

ull.crnativc

tca

dosage

form. In

this research, tea

will

be

formulated

to

be

granules

of

effervescent

which

is

only

need water

to drink. This

dosage

form

will

give

comfortable

feeling

for

consumen to

making

tl{eir

own

dosage

and

the dissolution

will

be more faster

in

hot or cold water.

Granules size

distribution

and

its

dissolved

time

are

important characteristic

in

effervescent system

which

will

control

bubbles

release.

homogenity,

flowability

and

disintegration effect.

Eksperimental

Material

:

Tea

leaves

(Camelliu

sinensis)

from

PTP

XII

Bantaran

-Blitar and

Wonosari Lawang, citric

acid,

bicarbonat natricurn.

alcohol

96%, PVP K-30. sucrosc.

Equipment

:

analytical

balance

(Sartorius

-

Germany). vacuum rotary

evaporator.

water

bath,

chrontatoglaphy

charnbcr,

rnoisturc

analyser

MA 30

(Sartorius

Germany),

volumemeter

(Erweka

-Germany), termometer,

glass equipment.

Methode

Herbs were standardized on its

organoleptic,

microscopic.

moisture
(7)

PROCEEDINCS OF

INTERNATIONAL SYMPOSIUM ON BIOMEDICINES

content

and

ashignition'

Tea

extract

was

extracted

by

maserating

tea

leaves

powder

with

alcohol

709lo as

solven,

using

vacuum

rotary

evaporator.

Granules

was

made

from

the

formulas

below. Fxtract

of

tea

and saccharum

lactis were mixed,

sieved by siever mesh 40 anddried

with

oven

at

50u

C. Half

of

dried extract

were

mixed with citric

acid,

preservatives

that

solved

in

alcohol

90%,

half of

PVP

K-30,

gmulized bY siever mesh 18. dried

wilh

oven, as an acid phase.

Base phase

was

made

from

half of

dried

extract,

natrium

bicarbonas,

aspartam,

and

half

of

PVP

K-30,

Granules

evaluation

showed

that

flow

time,

angle

of

repose and

moisture content

fulfilled

the

granulized

by

siever mesh 18, dried

with

oven. The gramiles product were evaluated

on its

flowability,

angle

of

repose, moisture content granule size' distribution and dissolved time' Results

In

this

research.

tea

was

collected

from

PTP)

(ll

which

is

processed

to

black tea. Determination

result

from

Purwodadi

Botanical Garden

show

that this

herb

used in this research was tea.

Herbs were standardized on its organoleptic, microscopis and purity.

The

result

showed

that

this

herbs fulfi lled the requirement.

requirements.

It

means

that

it

is

not

difficult

to process granules

with

high speed machine.

Anova

statistical test Tabel 1 . of Formula

Material Formulas

I

II

III

IV

Extract oftea

Citric acid arrhydrous

Bicmbonat natricus PVP K-30

Aspartam

Methyl Paraben

Propyl paraben

Saccharum lactis

100/0

12,sYo | sYo lVo

0,l 80/0

0,02% ad 100%

100/0

lz,5%

| 5v.

0,50

tyo 0,I 80/0 0,02%

ad | 00%

r00/0

12j%

t5%

lYo lYo 0, | 80/0

0.02% ad 100%

t00/0 12,5% | sV:o zYo lYo 0,I 80/0 oP020/0 ad 100%

Table 2. Evaluation

ofherbs

Evaluation Standard Result

Moisture content

Ashignition

<

10,0 yo <7,00/o

9.40%

6.48%

Table 3. Evaluation

of

Evaluation Standard FI f/ F3 F.l

Flow time (second)

Angle of repose(')

Moisture content (o )

0 granul -dg (tt) Dissolve time (min)

<

l0

25-40-<

ltJ%o

t.t

7,63+0,t2

32,I 0+ 1,37

9,0tJ+0,14

45 | ,4+20,7 7

I ,l9+0,04

7,53+0,06

33.5 l+ 1,28

8,49+0,68

435,93+26,7 6 1,48+0,07

7,90+0, I 0

34, I t+ 1,58

9,09+0,73

1,74+0,32

7,27+0,06 34,82+1,2

I

9,5 t+0,50

500;04+3,

00

)

la+

0, l3

(8)

PROCEEDTNCS OF

INTERNATIONAL SYMPOSIUM ON BIOMEDICINES

for

diameter

of

granules

shows

a

significant

difference

between

formulas. Analyzing

result

with

Honestly

Significant

Difference

(HSD) sYo

shows

a

significant difference between formula.

The

dissolve

time

evaluation

shows

that

FIV

does

not

fulfill

the

requirement.

There

is a

significant

difference

using

anova

statistical

method.

Analyzing

result

with

Honestly Significant

Difference

(HSD)

5%

shows

that

there

is

no

significant

difference between

FI

and

FIL

The diameter

of

granules and

its

dissolve

time,

formula

Il

with

0,5% PVP

K-30

as binder

give

a

better result. Conclusion

Granules Effervescent

Tea

with

A,5oA PVP

K-3 0

as binder

give

a better

result.

The best

formula

of

granules

effervecent

tea

is

obtained

with

0,5%

pVpK-30

as a binder.

References

Adisewojo

,S.,

1982.

Bercocok

Tanam Teh. penerbit

Sumur Bandung, Bandung, 19 - 22

Astuti, M,, 2001.

Makanan

fungsional

dan

dampaknya

bagi

kesehatan

:

potensi

antioksidan pada the. Seminar

On

Tea

and Health.

Fakultas

Telmologi

Pertanian UWM,

Surabaya,

l-7

Bandelin, F.J, Shangraw,

R.F.,

1992.

Compressed

tablet

by

wet granulation,.

In

:

Liebermann,

H.A,

Lachman,

L

(Ed)

Pharmaceutical

Dosage

Form:

Tablets. Vol

L

Marcell

Dekker,

Inc., New

york,

pp.

205 -209

Cartensen,

J.T and ping,

C.C.,

1977. Flow rate and repose angles

of

wet

processed granulation. J.

Pharm.Sci., I -30, 5 2-66

Hamdun,

F.,

Jonosewojo,

A.

2001.

Radikal

bebas, kesehatan dan

penyakit Seminar On Tea and

Health,

Fakultas

Telmologi

Pertanian

UWK

Surabava.

I-2

B i op har m ac a Res e ar c h g "

r!

"^I- B og,or A gr i cul tur a I U n iv ers ity

Bogor, lndonesiq, Ig,h _ I/h September 2003

Gambar

Tabel 1 .of FormulaMaterialFormulas

Referensi

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